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rs149595793

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149595793(A;A)
Make rs149595793(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70492544
GeneDLG3
is asnp
is mentioned by
dbSNPrs149595793
ebirs149595793
HLIrs149595793
Exacrs149595793
Varsomers149595793
Maprs149595793
PheGenIrs149595793
hapmaprs149595793
1000 genomesrs149595793
hgdprs149595793
ensemblrs149595793
gopubmedrs149595793
geneviewrs149595793
scholarrs149595793
googlers149595793
pharmgkbrs149595793
gwascentralrs149595793
openSNPrs149595793
23andMers149595793
23andMe allrs149595793
SNP Nexus

SNPshotrs149595793
SNPdbers149595793
MSV3drs149595793
GWAS Ctlgrs149595793
Max Magnitude0
ClinVar
Risk rs149595793(A;A)
Alt rs149595793(A;A)
Reference rs149595793(G;G)
Significance Probable-Pathogenic
Disease X-Linked mental retardation 90
Variation info
Gene DLG3
CLNDBN X-Linked mental retardation 90
Reversed 0
HGVS NC_000023.10:g.69712394G>A
CLNSRC
CLNACC RCV000209901.1,