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rs121913388

From SNPedia

OMIM600160
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913388(G,T;G,T)
Alt rs121913388(G,T;G,T)
Reference rs121913388(C;C)
Significance Other
Disease Melanoma
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, susceptibility to, 2
Reversed 1
HGVS NC_000009.11:g.21971120G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010012.2,


[PMID 21499247OA-icon.png] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.