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rs137854599

From SNPedia

OMIM600160
Desc
Variant0019
Relatedalso
ClinVar
Risk rs137854599(A;A)
Alt rs137854599(A;A)
Reference rs137854599(G;G)
Significance Other
Disease Melanoma Hereditary cutaneous melanoma Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, susceptibility to, 2 Hereditary cutaneous melanoma Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000009.11:g.21971092C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010033.2, RCV000122946.1, RCV000219725.1,