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rs587777327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777327(C;T)
Make rs587777327(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position9470735
GeneSETD5
is asnp
is mentioned by
dbSNPrs587777327
ebirs587777327
HLIrs587777327
Exacrs587777327
Varsomers587777327
Maprs587777327
PheGenIrs587777327
hapmaprs587777327
1000 genomesrs587777327
hgdprs587777327
ensemblrs587777327
gopubmedrs587777327
geneviewrs587777327
scholarrs587777327
googlers587777327
pharmgkbrs587777327
gwascentralrs587777327
openSNPrs587777327
23andMers587777327
23andMe allrs587777327
SNP Nexus

SNPshotrs587777327
SNPdbers587777327
MSV3drs587777327
GWAS Ctlgrs587777327
Max Magnitude0
ClinVar
Risk rs587777327(T;T)
Alt rs587777327(T;T)
Reference rs587777327(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene SETD5
CLNDBN Mental retardation, autosomal dominant 23
Reversed 0
HGVS NC_000003.11:g.9512419C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000114962.2,