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rs876660436

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660436(C;G)
Make rs876660436(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position21971025
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs876660436
ebirs876660436
HLIrs876660436
Exacrs876660436
Varsomers876660436
Maprs876660436
PheGenIrs876660436
hapmaprs876660436
1000 genomesrs876660436
hgdprs876660436
ensemblrs876660436
gopubmedrs876660436
geneviewrs876660436
scholarrs876660436
googlers876660436
pharmgkbrs876660436
gwascentralrs876660436
openSNPrs876660436
23andMers876660436
23andMe allrs876660436
SNP Nexus

SNPshotrs876660436
SNPdbers876660436
MSV3drs876660436
GWAS Ctlgrs876660436
Max Magnitude0
ClinVar
Risk rs876660436(G;G)
Alt rs876660436(G;G)
Reference rs876660436(C;C)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDKN2A
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000009.11:g.21971024G>C
CLNSRC
CLNACC RCV000213802.1,