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rs786202098

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202098(A;G)
Make rs786202098(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position6002638
GenePMS2
is asnp
is mentioned by
dbSNPrs786202098
ebirs786202098
HLIrs786202098
Exacrs786202098
Varsomers786202098
Maprs786202098
PheGenIrs786202098
hapmaprs786202098
1000 genomesrs786202098
hgdprs786202098
ensemblrs786202098
gopubmedrs786202098
geneviewrs786202098
scholarrs786202098
googlers786202098
pharmgkbrs786202098
gwascentralrs786202098
openSNPrs786202098
23andMers786202098
23andMe allrs786202098
SNP Nexus

SNPshotrs786202098
SNPdbers786202098
MSV3drs786202098
GWAS Ctlgrs786202098
Max Magnitude0
ClinVar
Risk rs786202098(G;G)
Alt rs786202098(G;G)
Reference rs786202098(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PMS2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000007.13:g.6042269T>C
CLNSRC
CLNACC RCV000164744.1,