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rs63751140

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751140(C;C)
Make rs63751140(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47471062
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751140
ebirs63751140
HLIrs63751140
Exacrs63751140
Varsomers63751140
Maprs63751140
PheGenIrs63751140
hapmaprs63751140
1000 genomesrs63751140
hgdprs63751140
ensemblrs63751140
gopubmedrs63751140
geneviewrs63751140
scholarrs63751140
googlers63751140
pharmgkbrs63751140
gwascentralrs63751140
openSNPrs63751140
23andMers63751140
23andMe allrs63751140
SNP Nexus

SNPshotrs63751140
SNPdbers63751140
MSV3drs63751140
GWAS Ctlgrs63751140
Max Magnitude0
ClinVar
Risk rs63751140(C;C)
Alt rs63751140(C;C)
Reference rs63751140(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698201G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076270.2,