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rs28936077

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28936077(C;C)
Make rs28936077(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position25015640
GeneARX
is asnp
is mentioned by
dbSNPrs28936077
ebirs28936077
HLIrs28936077
Exacrs28936077
Varsomers28936077
Maprs28936077
PheGenIrs28936077
hapmaprs28936077
1000 genomesrs28936077
hgdprs28936077
ensemblrs28936077
gopubmedrs28936077
geneviewrs28936077
scholarrs28936077
googlers28936077
pharmgkbrs28936077
gwascentralrs28936077
openSNPrs28936077
23andMers28936077
23andMe allrs28936077
SNP Nexus

SNPshotrs28936077
SNPdbers28936077
MSV3drs28936077
GWAS Ctlgrs28936077
Merged fromRs104894744
Max Magnitude0
OMIM300382
DescMENTAL RETARDATION, X-LINKED 54
Variant0013
Relatedalso
Neighborrs28936075
Distance2640
ClinVar
Risk rs28936077(C;C)
Alt rs28936077(C;C)
Reference rs28936077(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARX
CLNDBN Mental retardation, with or without seizures, ARX-related, X-linked
Reversed 1
HGVS NC_000023.10:g.25033757A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011949.18,