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

rs878853148

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853148(C;C)
Make rs878853148(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position54002150
GenePHF8
is asnp
is mentioned by
dbSNPrs878853148
ebirs878853148
HLIrs878853148
Exacrs878853148
Varsomers878853148
Maprs878853148
PheGenIrs878853148
hapmaprs878853148
1000 genomesrs878853148
hgdprs878853148
ensemblrs878853148
gopubmedrs878853148
geneviewrs878853148
scholarrs878853148
googlers878853148
pharmgkbrs878853148
gwascentralrs878853148
openSNPrs878853148
23andMers878853148
23andMe allrs878853148
SNP Nexus

SNPshotrs878853148
SNPdbers878853148
MSV3drs878853148
GWAS Ctlgrs878853148
Max Magnitude0
ClinVar
Risk rs878853148(C;C)
Alt rs878853148(C;C)
Reference rs878853148(G;G)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene PHF8
CLNDBN Intellectual disability
Reversed 1
HGVS NC_000023.10:g.54028583C>G
CLNSRC
CLNACC RCV000224454.1,