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rs587777408

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777408(A;A)
Make rs587777408(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position686992
GeneDEAF1
is asnp
is mentioned by
dbSNPrs587777408
ebirs587777408
HLIrs587777408
Exacrs587777408
Varsomers587777408
Maprs587777408
PheGenIrs587777408
hapmaprs587777408
1000 genomesrs587777408
hgdprs587777408
ensemblrs587777408
gopubmedrs587777408
geneviewrs587777408
scholarrs587777408
googlers587777408
pharmgkbrs587777408
gwascentralrs587777408
openSNPrs587777408
23andMers587777408
23andMe allrs587777408
SNP Nexus

SNPshotrs587777408
SNPdbers587777408
MSV3drs587777408
GWAS Ctlgrs587777408
Max Magnitude0
ClinVar
Risk rs587777408(A,G;A,G)
Alt rs587777408(A,G;A,G)
Reference rs587777408(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DEAF1
CLNDBN Mental retardation, autosomal dominant 24
Reversed 1
HGVS NC_000011.9:g.686992G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000119806.3,