Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs587777326(-;-)
Make rs587777326(-;CA)
ReferenceGRCh38 38.1/142
Chromosome3
Position9448461
GeneSETD5
is asnp
is mentioned by
dbSNPrs587777326
ebirs587777326
HLIrs587777326
Exacrs587777326
Varsomers587777326
Maprs587777326
PheGenIrs587777326
hapmaprs587777326
1000 genomesrs587777326
hgdprs587777326
ensemblrs587777326
gopubmedrs587777326
geneviewrs587777326
scholarrs587777326
googlers587777326
pharmgkbrs587777326
gwascentralrs587777326
openSNPrs587777326
23andMers587777326
23andMe allrs587777326
SNP Nexus

SNPshotrs587777326
SNPdbers587777326
MSV3drs587777326
GWAS Ctlgrs587777326
Max Magnitude0
ClinVar
Risk rs587777326(;)
Alt rs587777326(;)
Reference rs587777326(CA;CA)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene SETD5
CLNDBN Mental retardation, autosomal dominant 23
Reversed 0
HGVS NC_000003.11:g.9490145_9490146delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000114961.2,