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rs63751018

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751018(G;G)
Make rs63751018(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478493
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751018
ebirs63751018
HLIrs63751018
Exacrs63751018
Varsomers63751018
Maprs63751018
PheGenIrs63751018
hapmaprs63751018
1000 genomesrs63751018
hgdprs63751018
ensemblrs63751018
gopubmedrs63751018
geneviewrs63751018
scholarrs63751018
googlers63751018
pharmgkbrs63751018
gwascentralrs63751018
openSNPrs63751018
23andMers63751018
23andMe allrs63751018
SNP Nexus

SNPshotrs63751018
SNPdbers63751018
MSV3drs63751018
GWAS Ctlgrs63751018
Max Magnitude0
ClinVar
Risk rs63751018(G;G)
Alt rs63751018(G;G)
Reference rs63751018(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705632T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076473.2,