Have questions? Visit https://www.reddit.com/r/SNPedia

rs786201590

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786201590(G;G)
Make rs786201590(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47475049
GeneMSH2
is asnp
is mentioned by
dbSNPrs786201590
ebirs786201590
HLIrs786201590
Exacrs786201590
Varsomers786201590
Maprs786201590
PheGenIrs786201590
hapmaprs786201590
1000 genomesrs786201590
hgdprs786201590
ensemblrs786201590
gopubmedrs786201590
geneviewrs786201590
scholarrs786201590
googlers786201590
pharmgkbrs786201590
gwascentralrs786201590
openSNPrs786201590
23andMers786201590
23andMe allrs786201590
SNP Nexus

SNPshotrs786201590
SNPdbers786201590
MSV3drs786201590
GWAS Ctlgrs786201590
Max Magnitude0
ClinVar
Risk rs786201590(G;G)
Alt rs786201590(G;G)
Reference rs786201590(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.47702188T>G
CLNSRC
CLNACC RCV000163932.1,