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

rs587778533

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs587778533(-;T)
Make rs587778533(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47803554
GeneMSH6
is asnp
is mentioned by
dbSNPrs587778533
ClinGenrs587778533
ebirs587778533
HLIrs587778533
Exacrs587778533
Varsomers587778533
Maprs587778533
PheGenIrs587778533
hapmaprs587778533
1000 genomesrs587778533
hgdprs587778533
ensemblrs587778533
gopubmedrs587778533
geneviewrs587778533
scholarrs587778533
googlers587778533
pharmgkbrs587778533
gwascentralrs587778533
openSNPrs587778533
23andMers587778533
23andMe allrs587778533
SNP Nexus

SNPshotrs587778533
SNPdbers587778533
MSV3drs587778533
GWAS Ctlgrs587778533
Max Magnitude0
ClinVar
Risk rs587778533(T;T)
Alt rs587778533(T;T)
Reference Rs587778533(;)
Significance Pathogenic
Disease not specified Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not specified Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48030698dupT
CLNSRC
CLNACC RCV000121582.1, RCV000130275.3,