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rs876659736

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659736(A;G)
Make rs876659736(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5995612
GenePMS2
is asnp
is mentioned by
dbSNPrs876659736
ebirs876659736
HLIrs876659736
Exacrs876659736
Varsomers876659736
Maprs876659736
PheGenIrs876659736
hapmaprs876659736
1000 genomesrs876659736
hgdprs876659736
ensemblrs876659736
gopubmedrs876659736
geneviewrs876659736
scholarrs876659736
googlers876659736
pharmgkbrs876659736
gwascentralrs876659736
openSNPrs876659736
23andMers876659736
23andMe allrs876659736
SNP Nexus

SNPshotrs876659736
SNPdbers876659736
MSV3drs876659736
GWAS Ctlgrs876659736
Max Magnitude0
ClinVar
Risk rs876659736(G;G)
Alt rs876659736(G;G)
Reference rs876659736(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PMS2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000007.13:g.6035243T>C
CLNSRC
CLNACC RCV000219153.1,