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rs63751110

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751110(C;C)
Make rs63751110(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410322
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751110
ebirs63751110
HLIrs63751110
Exacrs63751110
Varsomers63751110
Maprs63751110
PheGenIrs63751110
hapmaprs63751110
1000 genomesrs63751110
hgdprs63751110
ensemblrs63751110
gopubmedrs63751110
geneviewrs63751110
scholarrs63751110
googlers63751110
pharmgkbrs63751110
gwascentralrs63751110
openSNPrs63751110
23andMers63751110
23andMe allrs63751110
SNP Nexus

SNPshotrs63751110
SNPdbers63751110
MSV3drs63751110
GWAS Ctlgrs63751110
Max Magnitude0
ClinVar
Risk rs63751110(C;C)
Alt rs63751110(C;C)
Reference rs63751110(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637461T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076650.2,