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rs878853144

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853144(C;T)
Make rs878853144(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position53239213
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs878853144
ebirs878853144
HLIrs878853144
Exacrs878853144
Varsomers878853144
Maprs878853144
PheGenIrs878853144
hapmaprs878853144
1000 genomesrs878853144
hgdprs878853144
ensemblrs878853144
gopubmedrs878853144
geneviewrs878853144
scholarrs878853144
googlers878853144
pharmgkbrs878853144
gwascentralrs878853144
openSNPrs878853144
23andMers878853144
23andMe allrs878853144
SNP Nexus

SNPshotrs878853144
SNPdbers878853144
MSV3drs878853144
GWAS Ctlgrs878853144
Max Magnitude0
ClinVar
Risk rs878853144(T;T)
Alt rs878853144(T;T)
Reference rs878853144(C;C)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene IQSEC2
CLNDBN Intellectual disability
Reversed 1
HGVS NC_000023.10:g.53268395G>A
CLNSRC
CLNACC RCV000224400.1,