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rs876658862

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658862(C;T)
Make rs876658862(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5987567
GenePMS2
is asnp
is mentioned by
dbSNPrs876658862
ebirs876658862
HLIrs876658862
Exacrs876658862
Varsomers876658862
Maprs876658862
PheGenIrs876658862
hapmaprs876658862
1000 genomesrs876658862
hgdprs876658862
ensemblrs876658862
gopubmedrs876658862
geneviewrs876658862
scholarrs876658862
googlers876658862
pharmgkbrs876658862
gwascentralrs876658862
openSNPrs876658862
23andMers876658862
23andMe allrs876658862
SNP Nexus

SNPshotrs876658862
SNPdbers876658862
MSV3drs876658862
GWAS Ctlgrs876658862
Max Magnitude0
ClinVar
Risk rs876658862(T;T)
Alt rs876658862(T;T)
Reference rs876658862(C;C)
Significance 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.6027198G>A
CLNSRC
CLNACC RCV000220993.1,