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rs786203704

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203704(-;-)
Make rs786203704(-;G)
Make rs786203704(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47475068
GeneMSH2
is asnp
is mentioned by
dbSNPrs786203704
ebirs786203704
HLIrs786203704
Exacrs786203704
Varsomers786203704
Maprs786203704
PheGenIrs786203704
hapmaprs786203704
1000 genomesrs786203704
hgdprs786203704
ensemblrs786203704
gopubmedrs786203704
geneviewrs786203704
scholarrs786203704
googlers786203704
pharmgkbrs786203704
gwascentralrs786203704
openSNPrs786203704
23andMers786203704
23andMe allrs786203704
SNP Nexus

SNPshotrs786203704
SNPdbers786203704
MSV3drs786203704
GWAS Ctlgrs786203704
Max Magnitude0
ClinVar
Risk rs786203704(G;G)
Alt rs786203704(G;G)
Reference rs786203704(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47702207dupG
CLNSRC
CLNACC RCV000167124.1,