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rs587777409

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777409(G;G)
Make rs587777409(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position686900
GeneDEAF1
is asnp
is mentioned by
dbSNPrs587777409
ebirs587777409
HLIrs587777409
Exacrs587777409
Varsomers587777409
Maprs587777409
PheGenIrs587777409
hapmaprs587777409
1000 genomesrs587777409
hgdprs587777409
ensemblrs587777409
gopubmedrs587777409
geneviewrs587777409
scholarrs587777409
googlers587777409
pharmgkbrs587777409
gwascentralrs587777409
openSNPrs587777409
23andMers587777409
23andMe allrs587777409
SNP Nexus

SNPshotrs587777409
SNPdbers587777409
MSV3drs587777409
GWAS Ctlgrs587777409
Max Magnitude0
ClinVar
Risk rs587777409(G,T;G,T)
Alt rs587777409(G,T;G,T)
Reference rs587777409(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DEAF1
CLNDBN Mental retardation, autosomal dominant 24
Reversed 1
HGVS NC_000011.9:g.686900T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000119807.2,