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rs876659900

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659900(C;T)
Make rs876659900(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5982861
GenePMS2
is asnp
is mentioned by
dbSNPrs876659900
ebirs876659900
HLIrs876659900
Exacrs876659900
Varsomers876659900
Maprs876659900
PheGenIrs876659900
hapmaprs876659900
1000 genomesrs876659900
hgdprs876659900
ensemblrs876659900
gopubmedrs876659900
geneviewrs876659900
scholarrs876659900
googlers876659900
pharmgkbrs876659900
gwascentralrs876659900
openSNPrs876659900
23andMers876659900
23andMe allrs876659900
SNP Nexus

SNPshotrs876659900
SNPdbers876659900
MSV3drs876659900
GWAS Ctlgrs876659900
Max Magnitude0
ClinVar
Risk rs876659900(T;T)
Alt rs876659900(T;T)
Reference Rs876659900(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PMS2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000007.13:g.6022492G>A
CLNSRC
CLNACC RCV000216032.1,