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rs267607930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607930(G;G)
Make rs267607930(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412411
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607930
ebirs267607930
HLIrs267607930
Exacrs267607930
Varsomers267607930
Maprs267607930
PheGenIrs267607930
hapmaprs267607930
1000 genomesrs267607930
hgdprs267607930
ensemblrs267607930
gopubmedrs267607930
geneviewrs267607930
scholarrs267607930
googlers267607930
pharmgkbrs267607930
gwascentralrs267607930
openSNPrs267607930
23andMers267607930
23andMe allrs267607930
SNP Nexus

SNPshotrs267607930
SNPdbers267607930
MSV3drs267607930
GWAS Ctlgrs267607930
Max Magnitude0
ClinVar
Risk rs267607930(C,G;C,G)
Alt rs267607930(C,G;C,G)
Reference rs267607930(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639550T>C; NC_000002.11:g.47639550T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000203689.1, RCV000076666.2,