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rs63751169

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63751169(-;-)
Make rs63751169(-;G)
Make rs63751169(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429857
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751169
ebirs63751169
HLIrs63751169
Exacrs63751169
Varsomers63751169
Maprs63751169
PheGenIrs63751169
hapmaprs63751169
1000 genomesrs63751169
hgdprs63751169
ensemblrs63751169
gopubmedrs63751169
geneviewrs63751169
scholarrs63751169
googlers63751169
pharmgkbrs63751169
gwascentralrs63751169
openSNPrs63751169
23andMers63751169
23andMe allrs63751169
SNP Nexus

SNPshotrs63751169
SNPdbers63751169
MSV3drs63751169
GWAS Ctlgrs63751169
Max Magnitude0
ClinVar
Risk rs63751169(G;G)
Alt rs63751169(G;G)
Reference rs63751169(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656996dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076057.2,