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rs63751317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751317(C;G)
Make rs63751317(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475233
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751317
ebirs63751317
HLIrs63751317
Exacrs63751317
Varsomers63751317
Maprs63751317
PheGenIrs63751317
hapmaprs63751317
1000 genomesrs63751317
hgdprs63751317
ensemblrs63751317
gopubmedrs63751317
geneviewrs63751317
scholarrs63751317
googlers63751317
pharmgkbrs63751317
gwascentralrs63751317
openSNPrs63751317
23andMers63751317
23andMe allrs63751317
SNP Nexus

SNPshotrs63751317
SNPdbers63751317
MSV3drs63751317
GWAS Ctlgrs63751317
Max Magnitude0
ClinVar
Risk rs63751317(G;G)
Alt rs63751317(G;G)
Reference rs63751317(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702372C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076327.2,