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rs587782638

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs587782638(-;-)
Make rs587782638(-;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799883
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782638
ebirs587782638
HLIrs587782638
Exacrs587782638
Varsomers587782638
Maprs587782638
PheGenIrs587782638
hapmaprs587782638
1000 genomesrs587782638
hgdprs587782638
ensemblrs587782638
gopubmedrs587782638
geneviewrs587782638
scholarrs587782638
googlers587782638
pharmgkbrs587782638
gwascentralrs587782638
openSNPrs587782638
23andMers587782638
23andMe allrs587782638
SNP Nexus

SNPshotrs587782638
SNPdbers587782638
MSV3drs587782638
GWAS Ctlgrs587782638
Max Magnitude0
ClinVar
Risk rs587782638(;)
Alt rs587782638(;)
Reference rs587782638(TT;TT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027022_48027023delTT
CLNSRC
CLNACC RCV000132031.2,