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rs876661113

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661113(G;T)
Make rs876661113(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5977587
GenePMS2
is asnp
is mentioned by
dbSNPrs876661113
ebirs876661113
HLIrs876661113
Exacrs876661113
Varsomers876661113
Maprs876661113
PheGenIrs876661113
hapmaprs876661113
1000 genomesrs876661113
hgdprs876661113
ensemblrs876661113
gopubmedrs876661113
geneviewrs876661113
scholarrs876661113
googlers876661113
pharmgkbrs876661113
gwascentralrs876661113
openSNPrs876661113
23andMers876661113
23andMe allrs876661113
SNP Nexus

SNPshotrs876661113
SNPdbers876661113
MSV3drs876661113
GWAS Ctlgrs876661113
Max Magnitude0
ClinVar
Risk rs876661113(C,T;C,T)
Alt rs876661113(C,T;C,T)
Reference rs876661113(G;G)
Significance Pathogenic
Disease not provided Lynch syndrome
Variation info
Gene PMS2
CLNDBN not provided Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6017218C>A; NC_000007.13:g.6017218C>G
CLNSRC
CLNACC RCV000219334.1, RCV000228982.1, RCV000234016.1,