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rs587781931

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781931(-;-)
Make rs587781931(-;A)
Make rs587781931(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position65077974
GeneMAX
is asnp
is mentioned by
dbSNPrs587781931
ebirs587781931
HLIrs587781931
Exacrs587781931
Varsomers587781931
Maprs587781931
PheGenIrs587781931
hapmaprs587781931
1000 genomesrs587781931
hgdprs587781931
ensemblrs587781931
gopubmedrs587781931
geneviewrs587781931
scholarrs587781931
googlers587781931
pharmgkbrs587781931
gwascentralrs587781931
openSNPrs587781931
23andMers587781931
23andMe allrs587781931
SNP Nexus

SNPshotrs587781931
SNPdbers587781931
MSV3drs587781931
GWAS Ctlgrs587781931
Max Magnitude0
ClinVar
Risk rs587781931(A;A)
Alt rs587781931(A;A)
Reference rs587781931(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MAX
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000014.8:g.65544693dupT
CLNSRC
CLNACC RCV000130290.2,