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

rs267607188

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607188(C;T)
Make rs267607188(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position53254856
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs267607188
ebirs267607188
HLIrs267607188
Exacrs267607188
Varsomers267607188
Maprs267607188
PheGenIrs267607188
hapmaprs267607188
1000 genomesrs267607188
hgdprs267607188
ensemblrs267607188
gopubmedrs267607188
geneviewrs267607188
scholarrs267607188
googlers267607188
pharmgkbrs267607188
gwascentralrs267607188
openSNPrs267607188
23andMers267607188
23andMe allrs267607188
SNP Nexus

SNPshotrs267607188
SNPdbers267607188
MSV3drs267607188
GWAS Ctlgrs267607188
Max Magnitude0
ClinVar
Risk rs267607188(T;T)
Alt rs267607188(T;T)
Reference rs267607188(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene IQSEC2
CLNDBN Mental retardation, X-linked 1
Reversed 1
HGVS NC_000023.10:g.53284038G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011612.4,