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rs267607950

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607950(G;T)
Make rs267607950(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429942
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607950
ebirs267607950
HLIrs267607950
Exacrs267607950
Varsomers267607950
Maprs267607950
PheGenIrs267607950
hapmaprs267607950
1000 genomesrs267607950
hgdprs267607950
ensemblrs267607950
gopubmedrs267607950
geneviewrs267607950
scholarrs267607950
googlers267607950
pharmgkbrs267607950
gwascentralrs267607950
openSNPrs267607950
23andMers267607950
23andMe allrs267607950
SNP Nexus

SNPshotrs267607950
SNPdbers267607950
MSV3drs267607950
GWAS Ctlgrs267607950
Max Magnitude0
ClinVar
Risk rs267607950(A,C,T;A,C,T)
Alt rs267607950(A,C,T;A,C,T)
Reference rs267607950(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657081G>A; NC_000002.11:g.47657081G>C; NC_000002.11:g.47657081G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076086.2, RCV000076087.2, RCV000076088.2,