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rs267607187

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607187(A;C)
Make rs267607187(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position53248778
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs267607187
ebirs267607187
HLIrs267607187
Exacrs267607187
Varsomers267607187
Maprs267607187
PheGenIrs267607187
hapmaprs267607187
1000 genomesrs267607187
hgdprs267607187
ensemblrs267607187
gopubmedrs267607187
geneviewrs267607187
scholarrs267607187
googlers267607187
pharmgkbrs267607187
gwascentralrs267607187
openSNPrs267607187
23andMers267607187
23andMe allrs267607187
SNP Nexus

SNPshotrs267607187
SNPdbers267607187
MSV3drs267607187
GWAS Ctlgrs267607187
Max Magnitude0
ClinVar
Risk rs267607187(C;C)
Alt rs267607187(C;C)
Reference rs267607187(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene IQSEC2
CLNDBN Mental retardation, X-linked 18
Reversed 1
HGVS NC_000023.10:g.53277960T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011610.9,