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rs587782326

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782326(-;-)
Make rs587782326(-;A)
Make rs587782326(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806629
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs587782326
ebirs587782326
HLIrs587782326
Exacrs587782326
Varsomers587782326
Maprs587782326
PheGenIrs587782326
hapmaprs587782326
1000 genomesrs587782326
hgdprs587782326
ensemblrs587782326
gopubmedrs587782326
geneviewrs587782326
scholarrs587782326
googlers587782326
pharmgkbrs587782326
gwascentralrs587782326
openSNPrs587782326
23andMers587782326
23andMe allrs587782326
SNP Nexus

SNPshotrs587782326
SNPdbers587782326
MSV3drs587782326
GWAS Ctlgrs587782326
Max Magnitude0
ClinVar
Risk rs587782326(A;A)
Alt rs587782326(A;A)
Reference rs587782326(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48033768dupA
CLNSRC
CLNACC RCV000131234.2,