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rs128624220

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128624220(C;T)
Make rs128624220(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153736372
GeneABCD1
is asnp
is mentioned by
dbSNPrs128624220
ebirs128624220
HLIrs128624220
Exacrs128624220
Varsomers128624220
Maprs128624220
PheGenIrs128624220
hapmaprs128624220
1000 genomesrs128624220
hgdprs128624220
ensemblrs128624220
gopubmedrs128624220
geneviewrs128624220
scholarrs128624220
googlers128624220
pharmgkbrs128624220
gwascentralrs128624220
openSNPrs128624220
23andMers128624220
23andMe allrs128624220
SNP Nexus

SNPshotrs128624220
SNPdbers128624220
MSV3drs128624220
GWAS Ctlgrs128624220
Max Magnitude0
OMIM300371
Desc
Variant0010
Relatedalso
ClinVar
Risk rs128624220(T;T)
Alt rs128624220(T;T)
Reference rs128624220(C;C)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153001826C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012053.2,