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rs63751411

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751411(G;T)
Make rs63751411(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47471041
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751411
ebirs63751411
HLIrs63751411
Exacrs63751411
Varsomers63751411
Maprs63751411
PheGenIrs63751411
hapmaprs63751411
1000 genomesrs63751411
hgdprs63751411
ensemblrs63751411
gopubmedrs63751411
geneviewrs63751411
scholarrs63751411
googlers63751411
pharmgkbrs63751411
gwascentralrs63751411
openSNPrs63751411
23andMers63751411
23andMe allrs63751411
SNP Nexus

SNPshotrs63751411
SNPdbers63751411
MSV3drs63751411
GWAS Ctlgrs63751411
Max Magnitude0
ClinVar
Risk rs63751411(T;T)
Alt rs63751411(T;T)
Reference rs63751411(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698180G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076261.2,