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rs587782593

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782593(A;T)
Make rs587782593(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800636
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782593
ebirs587782593
HLIrs587782593
Exacrs587782593
Varsomers587782593
Maprs587782593
PheGenIrs587782593
hapmaprs587782593
1000 genomesrs587782593
hgdprs587782593
ensemblrs587782593
gopubmedrs587782593
geneviewrs587782593
scholarrs587782593
googlers587782593
pharmgkbrs587782593
gwascentralrs587782593
openSNPrs587782593
23andMers587782593
23andMe allrs587782593
SNP Nexus

SNPshotrs587782593
SNPdbers587782593
MSV3drs587782593
GWAS Ctlgrs587782593
Max Magnitude0
ClinVar
Risk rs587782593(T;T)
Alt rs587782593(T;T)
Reference rs587782593(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027775A>T
CLNSRC
CLNACC RCV000131937.2,