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rs587777407

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777407(G;G)
Make rs587777407(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position686871
GeneDEAF1
is asnp
is mentioned by
dbSNPrs587777407
ebirs587777407
HLIrs587777407
Exacrs587777407
Varsomers587777407
Maprs587777407
PheGenIrs587777407
hapmaprs587777407
1000 genomesrs587777407
hgdprs587777407
ensemblrs587777407
gopubmedrs587777407
geneviewrs587777407
scholarrs587777407
googlers587777407
pharmgkbrs587777407
gwascentralrs587777407
openSNPrs587777407
23andMers587777407
23andMe allrs587777407
SNP Nexus

SNPshotrs587777407
SNPdbers587777407
MSV3drs587777407
GWAS Ctlgrs587777407
Max Magnitude0
ClinVar
Risk rs587777407(G,T;G,T)
Alt rs587777407(G,T;G,T)
Reference rs587777407(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DEAF1
CLNDBN Mental retardation, autosomal dominant 24
Reversed 1
HGVS NC_000011.9:g.686871T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000119805.2,