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

rs878853152

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs878853152(-;-)
Make rs878853152(-;CA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position120547154
GeneCUL4B
is asnp
is mentioned by
dbSNPrs878853152
ebirs878853152
HLIrs878853152
Exacrs878853152
Varsomers878853152
Maprs878853152
PheGenIrs878853152
hapmaprs878853152
1000 genomesrs878853152
hgdprs878853152
ensemblrs878853152
gopubmedrs878853152
geneviewrs878853152
scholarrs878853152
googlers878853152
pharmgkbrs878853152
gwascentralrs878853152
openSNPrs878853152
23andMers878853152
23andMe allrs878853152
SNP Nexus

SNPshotrs878853152
SNPdbers878853152
MSV3drs878853152
GWAS Ctlgrs878853152
Max Magnitude0
ClinVar
Risk rs878853152(;)
Alt rs878853152(;)
Reference rs878853152(CA;CA)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene CUL4B
CLNDBN Intellectual disability
Reversed 1
HGVS NC_000023.10:g.119681009_119681010delTG
CLNSRC
CLNACC RCV000224848.1,