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rs587777329

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777329(-;-)
Make rs587777329(-;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position9475618
GeneSETD5
is asnp
is mentioned by
dbSNPrs587777329
ebirs587777329
HLIrs587777329
Exacrs587777329
Varsomers587777329
Maprs587777329
PheGenIrs587777329
hapmaprs587777329
1000 genomesrs587777329
hgdprs587777329
ensemblrs587777329
gopubmedrs587777329
geneviewrs587777329
scholarrs587777329
googlers587777329
pharmgkbrs587777329
gwascentralrs587777329
openSNPrs587777329
23andMers587777329
23andMe allrs587777329
SNP Nexus

SNPshotrs587777329
SNPdbers587777329
MSV3drs587777329
GWAS Ctlgrs587777329
Max Magnitude0
ClinVar
Risk rs587777329(;)
Alt rs587777329(;)
Reference rs587777329(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene SETD5
CLNDBN Mental retardation, autosomal dominant 23
Reversed 0
HGVS NC_000003.11:g.9517302delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000114964.2,