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rs876660075

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660075(-;-)
Make rs876660075(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5991972
GenePMS2
is asnp
is mentioned by
dbSNPrs876660075
ebirs876660075
HLIrs876660075
Exacrs876660075
Varsomers876660075
Maprs876660075
PheGenIrs876660075
hapmaprs876660075
1000 genomesrs876660075
hgdprs876660075
ensemblrs876660075
gopubmedrs876660075
geneviewrs876660075
scholarrs876660075
googlers876660075
pharmgkbrs876660075
gwascentralrs876660075
openSNPrs876660075
23andMers876660075
23andMe allrs876660075
SNP Nexus

SNPshotrs876660075
SNPdbers876660075
MSV3drs876660075
GWAS Ctlgrs876660075
Max Magnitude0
ClinVar
Risk rs876660075(;)
Alt rs876660075(;)
Reference rs876660075(G;G)
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.6031603delC
CLNSRC
CLNACC RCV000216559.1,