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rs128624225

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128624225(C;T)
Make rs128624225(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153743023
GeneABCD1
is asnp
is mentioned by
dbSNPrs128624225
ebirs128624225
HLIrs128624225
Exacrs128624225
Varsomers128624225
Maprs128624225
PheGenIrs128624225
hapmaprs128624225
1000 genomesrs128624225
hgdprs128624225
ensemblrs128624225
gopubmedrs128624225
geneviewrs128624225
scholarrs128624225
googlers128624225
pharmgkbrs128624225
gwascentralrs128624225
openSNPrs128624225
23andMers128624225
23andMe allrs128624225
SNP Nexus

SNPshotrs128624225
SNPdbers128624225
MSV3drs128624225
GWAS Ctlgrs128624225
Max Magnitude0
OMIM300371
Desc
Variant0019
Relatedalso
ClinVar
Risk rs128624225(T;T)
Alt rs128624225(T;T)
Reference rs128624225(C;C)
Significance Pathogenic
Disease Addison's disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Addison's disease Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153008477C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012062.17, RCV000180094.1,