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rs267607186

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607186(C;T)
Make rs267607186(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position53247131
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs267607186
ebirs267607186
HLIrs267607186
Exacrs267607186
Varsomers267607186
Maprs267607186
PheGenIrs267607186
hapmaprs267607186
1000 genomesrs267607186
hgdprs267607186
ensemblrs267607186
gopubmedrs267607186
geneviewrs267607186
scholarrs267607186
googlers267607186
pharmgkbrs267607186
gwascentralrs267607186
openSNPrs267607186
23andMers267607186
23andMe allrs267607186
SNP Nexus

SNPshotrs267607186
SNPdbers267607186
MSV3drs267607186
GWAS Ctlgrs267607186
Max Magnitude0
ClinVar
Risk rs267607186(T;T)
Alt rs267607186(T;T)
Reference rs267607186(C;C)
Significance Pathogenic
Disease Mental retardation not provided
Variation info
Gene IQSEC2
CLNDBN Mental retardation, X-linked 1 not provided
Reversed 1
HGVS NC_000023.10:g.53276313G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011609.2, RCV000180207.1,