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rs45476696

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45476696(A;A)
Make rs45476696(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position21970902
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs45476696
ebirs45476696
HLIrs45476696
Exacrs45476696
Varsomers45476696
Maprs45476696
PheGenIrs45476696
hapmaprs45476696
1000 genomesrs45476696
hgdprs45476696
ensemblrs45476696
gopubmedrs45476696
geneviewrs45476696
scholarrs45476696
googlers45476696
pharmgkbrs45476696
gwascentralrs45476696
openSNPrs45476696
23andMers45476696
23andMe allrs45476696
SNP Nexus

SNPshotrs45476696
SNPdbers45476696
MSV3drs45476696
GWAS Ctlgrs45476696
Max Magnitude0
ClinVar
Risk rs45476696(A,T;A,T)
Alt rs45476696(A,T;A,T)
Reference rs45476696(G;G)
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.21970901C>A
CLNSRC
CLNACC RCV000198192.2, RCV000223581.1,