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rs63751712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751712(G;T)
Make rs63751712(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429929
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751712
ebirs63751712
HLIrs63751712
Exacrs63751712
Varsomers63751712
Maprs63751712
PheGenIrs63751712
hapmaprs63751712
1000 genomesrs63751712
hgdprs63751712
ensemblrs63751712
gopubmedrs63751712
geneviewrs63751712
scholarrs63751712
googlers63751712
pharmgkbrs63751712
gwascentralrs63751712
openSNPrs63751712
23andMers63751712
23andMe allrs63751712
SNP Nexus

SNPshotrs63751712
SNPdbers63751712
MSV3drs63751712
GWAS Ctlgrs63751712
Max Magnitude0
ClinVar
Risk rs63751712(T;T)
Alt rs63751712(T;T)
Reference rs63751712(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657068G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076083.2,