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rs128624216

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs128624216(A;G)
Make rs128624216(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153725709
GeneABCD1, BCAP31
is asnp
is mentioned by
dbSNPrs128624216
ebirs128624216
HLIrs128624216
Exacrs128624216
Varsomers128624216
Maprs128624216
PheGenIrs128624216
hapmaprs128624216
1000 genomesrs128624216
hgdprs128624216
ensemblrs128624216
gopubmedrs128624216
geneviewrs128624216
scholarrs128624216
googlers128624216
pharmgkbrs128624216
gwascentralrs128624216
openSNPrs128624216
23andMers128624216
23andMe allrs128624216
SNP Nexus

SNPshotrs128624216
SNPdbers128624216
MSV3drs128624216
GWAS Ctlgrs128624216
Max Magnitude0
OMIM300371
Desc
Variant0006
Relatedalso
ClinVar
Risk rs128624216(G;G)
Alt rs128624216(G;G)
Reference rs128624216(A;A)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene BCAP31 ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.152991164A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012049.2,