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rs267607974

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607974(-;-)
Make rs267607974(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47471020
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607974
ebirs267607974
HLIrs267607974
Exacrs267607974
Varsomers267607974
Maprs267607974
PheGenIrs267607974
hapmaprs267607974
1000 genomesrs267607974
hgdprs267607974
ensemblrs267607974
gopubmedrs267607974
geneviewrs267607974
scholarrs267607974
googlers267607974
pharmgkbrs267607974
gwascentralrs267607974
openSNPrs267607974
23andMers267607974
23andMe allrs267607974
SNP Nexus

SNPshotrs267607974
SNPdbers267607974
MSV3drs267607974
GWAS Ctlgrs267607974
Max Magnitude0
ClinVar
Risk rs267607974(;)
Alt rs267607974(;)
Reference rs267607974(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698159delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076256.2,