Variant (rsID / SNP)

rs370609910

rs370609910 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDK4. Location: chromosome 12, position 58,143,104. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CDK4Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:58143104
Cytoband: 12q14.1
HGVS: NM_005981.5(TSPAN31):c.*2031T>A
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Melanoma, cutaneous malignant, susceptibility to, 3|Familial melanoma

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.