Genetic Counselors

Healthcare Practitioners and Technical Occupations · Job Skills & Competencies · SOC 29-9092 · 44 skills

Occupation context

These O*NET tasks describe the occupation. They provide context for this SOC mapping, but do not mean every listed Skill performs every task.

Interpret laboratory results and communicate findings to patients or physicians.
Discuss testing options and the associated risks, benefits and limitations with patients and families to assist them in making informed decisions.
Analyze genetic information to identify patients or families at risk for specific disorders or syndromes.

O*NET task statements are shown in their source language (English). Task data excerpted from the O*NET® 29.1 Database (USDOL/ETA) and used under CC BY 4.0.

Representative sources

A bounded sample of popular skills mapped to this occupation, with at most one Skill from each GitHub repository. The complete mapped list follows.

clinpgx-database

davila7/claude-code-templates

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

clinpgx-database

foryourhealth111-pixel/Vibe-Skills

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

clinpgx-database

LeonChaoX/qinyan-academic-skills

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

variant-interpretation

lamm-mit/scienceclaw

ToolUniverse workflow — Variant Interpretation

All mapped skills

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Skill names and descriptions remain in the language supplied by their source repository.

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clinpgx-database

davila7/claude-code-templates

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

clinvar-database

davila7/claude-code-templates

Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.

clinpgx-database

foryourhealth111-pixel/Vibe-Skills

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

clinpgx-database

LeonChaoX/qinyan-academic-skills

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

variant-interpretation

lamm-mit/scienceclaw

ToolUniverse workflow — Variant Interpretation

clinpgx-database

swaruplab/operon

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

family-health-analyzer

分析家族病史、评估遗传风险、识别家庭健康模式、提供个性化预防建议

interpreting-genetic-testing

CaseMark/skills

Structures genetic test result interpretation with variant classification (ACMG criteria) and clinical actionability. Use when interpreting genetic results, classifying variants, or documenting genetic findings.

OpenVet-Projects/VetClaw

Query OMIA (Online Mendelian Inheritance in Animals) for inherited disorders and traits cataloged across species. The veterinary equivalent of OMIM. Use for genetic disease research and breed predisposition data.

interpreting-genomic-profiling

Structures comprehensive genomic profiling interpretation with actionable mutations and matched therapies. Use when reviewing genomic test results, identifying targeted therapy options, or interpreting NGS panels.

managing-hereditary-cancer-syndromes

Guides hereditary cancer risk assessment with genetic testing criteria and management recommendations. Use when evaluating hereditary cancer risk, ordering genetic testing, or managing high-risk patients.

genomic-variant-interpretation

awslabs/hcls-agent-skills

Reason about germline and somatic variant classification using ACMG/AMP 2015 and AMP/ASCO/CAP frameworks. Use when the user asks to classify a variant, interpret a VCF annotation, resolve a VUS, apply ACMG criteria, weigh ClinVar evidence, evaluate gnomAD allele frequencies, interpret REVEL/CADD/SpliceAI scores, decide whether PVS1 applies, or assess gene-disease validity before reporting. Triggers include "ACMG", "variant classification", "pathogenic", "likely pathogenic", "VUS", "benign", "ClinVar", "gnomAD", "REVEL", "CADD", "SpliceAI", "PVS1", "loss of function", "nonsense variant", "missense interpretation", "splice variant", "filtering allele frequency", "ClinGen", "somatic variant tier".