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rs267607696

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607696(-;-)
Make rs267607696(-;GG)
Make rs267607696(GG;GG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445611
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607696
ebirs267607696
HLIrs267607696
Exacrs267607696
Varsomers267607696
Maprs267607696
PheGenIrs267607696
hapmaprs267607696
1000 genomesrs267607696
hgdprs267607696
ensemblrs267607696
gopubmedrs267607696
geneviewrs267607696
scholarrs267607696
googlers267607696
pharmgkbrs267607696
gwascentralrs267607696
openSNPrs267607696
23andMers267607696
23andMe allrs267607696
SNP Nexus

SNPshotrs267607696
SNPdbers267607696
MSV3drs267607696
GWAS Ctlgrs267607696
Max Magnitude0
ClinVar
Risk rs267607696(GG;GG)
Alt rs267607696(GG;GG)
Reference rs267607696(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672750_47672751insGG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076127.2,