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

rs752738546

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752738546(A;A)
Make rs752738546(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41343802
GeneDDX3X
is asnp
is mentioned by
dbSNPrs752738546
ebirs752738546
HLIrs752738546
Exacrs752738546
Varsomers752738546
Maprs752738546
PheGenIrs752738546
hapmaprs752738546
1000 genomesrs752738546
hgdprs752738546
ensemblrs752738546
gopubmedrs752738546
geneviewrs752738546
scholarrs752738546
googlers752738546
pharmgkbrs752738546
gwascentralrs752738546
openSNPrs752738546
23andMers752738546
23andMe allrs752738546
SNP Nexus

SNPshotrs752738546
SNPdbers752738546
MSV3drs752738546
GWAS Ctlgrs752738546
Max Magnitude0
ClinVar
Risk rs752738546(A;A)
Alt rs752738546(A;A)
Reference rs752738546(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DDX3X
CLNDBN Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41203055G>T
CLNSRC
CLNACC RCV000209908.1,