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rs786203424

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203424(G;G)
Make rs786203424(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47414306
GeneMSH2
is asnp
is mentioned by
dbSNPrs786203424
ebirs786203424
HLIrs786203424
Exacrs786203424
Varsomers786203424
Maprs786203424
PheGenIrs786203424
hapmaprs786203424
1000 genomesrs786203424
hgdprs786203424
ensemblrs786203424
gopubmedrs786203424
geneviewrs786203424
scholarrs786203424
googlers786203424
pharmgkbrs786203424
gwascentralrs786203424
openSNPrs786203424
23andMers786203424
23andMe allrs786203424
SNP Nexus

SNPshotrs786203424
SNPdbers786203424
MSV3drs786203424
GWAS Ctlgrs786203424
Max Magnitude0
ClinVar
Risk rs786203424(G;G)
Alt rs786203424(G;G)
Reference rs786203424(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47641445T>G
CLNSRC
CLNACC RCV000166723.1,