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rs267607986

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607986(G;T)
Make rs267607986(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475271
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607986
ebirs267607986
HLIrs267607986
Exacrs267607986
Varsomers267607986
Maprs267607986
PheGenIrs267607986
hapmaprs267607986
1000 genomesrs267607986
hgdprs267607986
ensemblrs267607986
gopubmedrs267607986
geneviewrs267607986
scholarrs267607986
googlers267607986
pharmgkbrs267607986
gwascentralrs267607986
openSNPrs267607986
23andMers267607986
23andMe allrs267607986
SNP Nexus

SNPshotrs267607986
SNPdbers267607986
MSV3drs267607986
GWAS Ctlgrs267607986
Max Magnitude0
ClinVar
Risk rs267607986(A,C,T;A,C,T)
Alt rs267607986(A,C,T;A,C,T)
Reference rs267607986(G;G)
Significance Pathogenic
Disease Lynch syndrome Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47702410G>A; NC_000002.11:g.47702410G>C; NC_000002.11:g.47702410G>T
CLNSRC HGMD International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076337.2, RCV000078422.4, RCV000076338.2, RCV000076339.2, RCV000168730.1,