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rs797045594

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045594(-;-)
Make rs797045594(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
is asnp
is mentioned by
dbSNPrs797045594
ClinGenrs797045594
ebirs797045594
HLIrs797045594
Exacrs797045594
Varsomers797045594
Maprs797045594
PheGenIrs797045594
hapmaprs797045594
1000 genomesrs797045594
hgdprs797045594
ensemblrs797045594
gopubmedrs797045594
geneviewrs797045594
scholarrs797045594
googlers797045594
pharmgkbrs797045594
gwascentralrs797045594
openSNPrs797045594
23andMers797045594
23andMe allrs797045594
SNP Nexus

SNPshotrs797045594
SNPdbers797045594
MSV3drs797045594
GWAS Ctlgrs797045594
Max Magnitude0
ClinVar
Risk rs797045594(-;-)
Alt rs797045594(-;-)
Reference Rs797045594(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene GATAD2B
CLNDBN Mental retardation, autosomal dominant 18
Reversed 1
HGVS NC_000001.10:g.153788984delC
CLNSRC
CLNACC RCV000194804.1,