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rs864622636

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622636(C;T)
Make rs864622636(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position21974680
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs864622636
ebirs864622636
HLIrs864622636
Exacrs864622636
Varsomers864622636
Maprs864622636
PheGenIrs864622636
hapmaprs864622636
1000 genomesrs864622636
hgdprs864622636
ensemblrs864622636
gopubmedrs864622636
geneviewrs864622636
scholarrs864622636
googlers864622636
pharmgkbrs864622636
gwascentralrs864622636
openSNPrs864622636
23andMers864622636
23andMe allrs864622636
SNP Nexus

SNPshotrs864622636
SNPdbers864622636
MSV3drs864622636
GWAS Ctlgrs864622636
Max Magnitude0
ClinVar
Risk rs864622636(T;T)
Alt rs864622636(T;T)
Reference rs864622636(C;C)
Significance Pathogenic
Disease Hereditary cutaneous melanoma Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDKN2A
CLNDBN Hereditary cutaneous melanoma Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000009.11:g.21974679G>A
CLNSRC
CLNACC RCV000206296.2, RCV000221580.1,