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rs267607921

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs267607921(-;-)
Make rs267607921(-;TG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408444
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607921
ebirs267607921
HLIrs267607921
Exacrs267607921
Varsomers267607921
Maprs267607921
PheGenIrs267607921
hapmaprs267607921
1000 genomesrs267607921
hgdprs267607921
ensemblrs267607921
gopubmedrs267607921
geneviewrs267607921
scholarrs267607921
googlers267607921
pharmgkbrs267607921
gwascentralrs267607921
openSNPrs267607921
23andMers267607921
23andMe allrs267607921
SNP Nexus

SNPshotrs267607921
SNPdbers267607921
MSV3drs267607921
GWAS Ctlgrs267607921
Max Magnitude0
ClinVar
Risk rs267607921(;)
Alt rs267607921(;)
Reference rs267607921(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635583_47635584delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076503.2,