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rs587777328

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777328(-;-)
Make rs587777328(-;G)
Make rs587777328(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position9475533
GeneSETD5
is asnp
is mentioned by
dbSNPrs587777328
ebirs587777328
HLIrs587777328
Exacrs587777328
Varsomers587777328
Maprs587777328
PheGenIrs587777328
hapmaprs587777328
1000 genomesrs587777328
hgdprs587777328
ensemblrs587777328
gopubmedrs587777328
geneviewrs587777328
scholarrs587777328
googlers587777328
pharmgkbrs587777328
gwascentralrs587777328
openSNPrs587777328
23andMers587777328
23andMe allrs587777328
SNP Nexus

SNPshotrs587777328
SNPdbers587777328
MSV3drs587777328
GWAS Ctlgrs587777328
Max Magnitude0
ClinVar
Risk rs587777328(G;G)
Alt rs587777328(G;G)
Reference rs587777328(;)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene SETD5
CLNDBN Mental retardation, autosomal dominant 23
Reversed 0
HGVS NC_000003.11:g.9517217dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000114963.2,