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rs267607995

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607995(A;A)
Make rs267607995(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476408
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607995
ebirs267607995
HLIrs267607995
Exacrs267607995
Varsomers267607995
Maprs267607995
PheGenIrs267607995
hapmaprs267607995
1000 genomesrs267607995
hgdprs267607995
ensemblrs267607995
gopubmedrs267607995
geneviewrs267607995
scholarrs267607995
googlers267607995
pharmgkbrs267607995
gwascentralrs267607995
openSNPrs267607995
23andMers267607995
23andMe allrs267607995
SNP Nexus

SNPshotrs267607995
SNPdbers267607995
MSV3drs267607995
GWAS Ctlgrs267607995
Max Magnitude0
ClinVar
Risk rs267607995(A,T;A,T)
Alt rs267607995(A,T;A,T)
Reference rs267607995(G;G)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000002.11:g.47703547G>A; NC_000002.11:g.47703547G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076370.3, RCV000132039.2, RCV000202225.1, RCV000076371.2,