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rs587782111

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782111(-;-)
Make rs587782111(-;A)
Make rs587782111(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47804947
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782111
ebirs587782111
HLIrs587782111
Exacrs587782111
Varsomers587782111
Maprs587782111
PheGenIrs587782111
hapmaprs587782111
1000 genomesrs587782111
hgdprs587782111
ensemblrs587782111
gopubmedrs587782111
geneviewrs587782111
scholarrs587782111
googlers587782111
pharmgkbrs587782111
gwascentralrs587782111
openSNPrs587782111
23andMers587782111
23andMe allrs587782111
SNP Nexus

SNPshotrs587782111
SNPdbers587782111
MSV3drs587782111
GWAS Ctlgrs587782111
Max Magnitude0
ClinVar
Risk rs587782111(A;A)
Alt rs587782111(A;A)
Reference rs587782111(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48032086dupA
CLNSRC
CLNACC RCV000130627.2, RCV000202052.1,