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rs878853145

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853145(C;T)
Make rs878853145(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position48903017
GenePQBP1, SLC35A2
is asnp
is mentioned by
dbSNPrs878853145
ebirs878853145
HLIrs878853145
Exacrs878853145
Varsomers878853145
Maprs878853145
PheGenIrs878853145
hapmaprs878853145
1000 genomesrs878853145
hgdprs878853145
ensemblrs878853145
gopubmedrs878853145
geneviewrs878853145
scholarrs878853145
googlers878853145
pharmgkbrs878853145
gwascentralrs878853145
openSNPrs878853145
23andMers878853145
23andMe allrs878853145
SNP Nexus

SNPshotrs878853145
SNPdbers878853145
MSV3drs878853145
GWAS Ctlgrs878853145
Max Magnitude0
ClinVar
Risk rs878853145(T;T)
Alt rs878853145(T;T)
Reference rs878853145(C;C)
Significance Probable-Pathogenic
Disease Intellectual disability
Variation info
Gene PQBP1 SLC35A2
CLNDBN Intellectual disability
Reversed 0
HGVS NC_000023.10:g.48760294C>T
CLNSRC
CLNACC RCV000224749.1,