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rs786201066

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201066(C;T)
Make rs786201066(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47445622
GeneMSH2
is asnp
is mentioned by
dbSNPrs786201066
ebirs786201066
HLIrs786201066
Exacrs786201066
Varsomers786201066
Maprs786201066
PheGenIrs786201066
hapmaprs786201066
1000 genomesrs786201066
hgdprs786201066
ensemblrs786201066
gopubmedrs786201066
geneviewrs786201066
scholarrs786201066
googlers786201066
pharmgkbrs786201066
gwascentralrs786201066
openSNPrs786201066
23andMers786201066
23andMe allrs786201066
SNP Nexus

SNPshotrs786201066
SNPdbers786201066
MSV3drs786201066
GWAS Ctlgrs786201066
Max Magnitude0
ClinVar
Risk rs786201066(T;T)
Alt rs786201066(T;T)
Reference rs786201066(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47672761C>T
CLNSRC
CLNACC RCV000162487.1, RCV000202208.1,