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rs875989799

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989799(C;T)
Make rs875989799(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position53248814
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs875989799
ebirs875989799
HLIrs875989799
Exacrs875989799
Varsomers875989799
Maprs875989799
PheGenIrs875989799
hapmaprs875989799
1000 genomesrs875989799
hgdprs875989799
ensemblrs875989799
gopubmedrs875989799
geneviewrs875989799
scholarrs875989799
googlers875989799
pharmgkbrs875989799
gwascentralrs875989799
openSNPrs875989799
23andMers875989799
23andMe allrs875989799
SNP Nexus

SNPshotrs875989799
SNPdbers875989799
MSV3drs875989799
GWAS Ctlgrs875989799
Max Magnitude0
ClinVar
Risk rs875989799(T;T)
Alt rs875989799(T;T)
Reference rs875989799(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene IQSEC2
CLNDBN Mental retardation, X-linked 1
Reversed 1
HGVS NC_000023.10:g.53277996G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000211090.1,