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rs551060742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs551060742(C;T)
Make rs551060742(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position47482929
GeneMSH2
is asnp
is mentioned by
dbSNPrs551060742
ebirs551060742
HLIrs551060742
Exacrs551060742
Varsomers551060742
Maprs551060742
PheGenIrs551060742
hapmaprs551060742
1000 genomesrs551060742
hgdprs551060742
ensemblrs551060742
gopubmedrs551060742
geneviewrs551060742
scholarrs551060742
googlers551060742
pharmgkbrs551060742
gwascentralrs551060742
openSNPrs551060742
23andMers551060742
23andMe allrs551060742
SNP Nexus

SNPshotrs551060742
SNPdbers551060742
MSV3drs551060742
GWAS Ctlgrs551060742
Max Magnitude0
ClinVar
Risk rs551060742(T;T)
Alt rs551060742(T;T)
Reference rs551060742(C;C)
Significance Pathogenic
Disease Lynch syndrome not specified
Variation info
Gene MSH2
CLNDBN Lynch syndrome not specified
Reversed 0
HGVS NC_000002.11:g.47710068C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076547.3, RCV000236645.1,