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rs267608000

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs267608000(-;-)
Make rs267608000(-;GT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476382
GeneMSH2
is asnp
is mentioned by
dbSNPrs267608000
ebirs267608000
HLIrs267608000
Exacrs267608000
Varsomers267608000
Maprs267608000
PheGenIrs267608000
hapmaprs267608000
1000 genomesrs267608000
hgdprs267608000
ensemblrs267608000
gopubmedrs267608000
geneviewrs267608000
scholarrs267608000
googlers267608000
pharmgkbrs267608000
gwascentralrs267608000
openSNPrs267608000
23andMers267608000
23andMe allrs267608000
SNP Nexus

SNPshotrs267608000
SNPdbers267608000
MSV3drs267608000
GWAS Ctlgrs267608000
Max Magnitude0
ClinVar
Risk rs267608000(;)
Alt rs267608000(;)
Reference rs267608000(GT;GT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703521_47703522delGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076364.2,