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rs63751429

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751429(C;T)
Make rs63751429(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408466
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751429
ebirs63751429
HLIrs63751429
Exacrs63751429
Varsomers63751429
Maprs63751429
PheGenIrs63751429
hapmaprs63751429
1000 genomesrs63751429
hgdprs63751429
ensemblrs63751429
gopubmedrs63751429
geneviewrs63751429
scholarrs63751429
googlers63751429
pharmgkbrs63751429
gwascentralrs63751429
openSNPrs63751429
23andMers63751429
23andMe allrs63751429
SNP Nexus

SNPshotrs63751429
SNPdbers63751429
MSV3drs63751429
GWAS Ctlgrs63751429
Max Magnitude0
ClinVar
Risk rs63751429(T;T)
Alt rs63751429(T;T)
Reference rs63751429(C;C)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635605C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076546.2,