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rs786203604

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203604(-;-)
Make rs786203604(-;G)
Make rs786203604(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47414389
GeneMSH2
is asnp
is mentioned by
dbSNPrs786203604
ebirs786203604
HLIrs786203604
Exacrs786203604
Varsomers786203604
Maprs786203604
PheGenIrs786203604
hapmaprs786203604
1000 genomesrs786203604
hgdprs786203604
ensemblrs786203604
gopubmedrs786203604
geneviewrs786203604
scholarrs786203604
googlers786203604
pharmgkbrs786203604
gwascentralrs786203604
openSNPrs786203604
23andMers786203604
23andMe allrs786203604
SNP Nexus

SNPshotrs786203604
SNPdbers786203604
MSV3drs786203604
GWAS Ctlgrs786203604
Max Magnitude0
ClinVar
Risk rs786203604(G;G)
Alt rs786203604(G;G)
Reference rs786203604(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47641528dupG
CLNSRC
CLNACC RCV000166990.1,