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rs587776931

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776931(A;A)
Make rs587776931(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
is asnp
is mentioned by
dbSNPrs587776931
ebirs587776931
HLIrs587776931
Exacrs587776931
Varsomers587776931
Maprs587776931
PheGenIrs587776931
hapmaprs587776931
1000 genomesrs587776931
hgdprs587776931
ensemblrs587776931
gopubmedrs587776931
geneviewrs587776931
scholarrs587776931
googlers587776931
pharmgkbrs587776931
gwascentralrs587776931
openSNPrs587776931
23andMers587776931
23andMe allrs587776931
SNP Nexus

SNPshotrs587776931
SNPdbers587776931
MSV3drs587776931
GWAS Ctlgrs587776931
Max Magnitude0
ClinVar
Risk rs587776931(A;A)
Alt rs587776931(A;A)
Reference rs587776931(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene GATAD2B
CLNDBN Mental retardation, autosomal dominant 18
Reversed 0
HGVS NC_000001.10:g.153785737G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032869.3,