Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607956(G;T)
Make rs267607956(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463030
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607956
ebirs267607956
HLIrs267607956
Exacrs267607956
Varsomers267607956
Maprs267607956
PheGenIrs267607956
hapmaprs267607956
1000 genomesrs267607956
hgdprs267607956
ensemblrs267607956
gopubmedrs267607956
geneviewrs267607956
scholarrs267607956
googlers267607956
pharmgkbrs267607956
gwascentralrs267607956
openSNPrs267607956
23andMers267607956
23andMe allrs267607956
SNP Nexus

SNPshotrs267607956
SNPdbers267607956
MSV3drs267607956
GWAS Ctlgrs267607956
Max Magnitude0
ClinVar
Risk rs267607956(T;T)
Alt rs267607956(T;T)
Reference rs267607956(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690169G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076141.2,