Have questions? Visit https://www.reddit.com/r/SNPedia

rs128624213

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs128624213(A;A)
Make rs128624213(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153726137
GeneABCD1, BCAP31
is asnp
is mentioned by
dbSNPrs128624213
ebirs128624213
HLIrs128624213
Exacrs128624213
Varsomers128624213
Maprs128624213
PheGenIrs128624213
hapmaprs128624213
1000 genomesrs128624213
hgdprs128624213
ensemblrs128624213
gopubmedrs128624213
geneviewrs128624213
scholarrs128624213
googlers128624213
pharmgkbrs128624213
gwascentralrs128624213
openSNPrs128624213
23andMers128624213
23andMe allrs128624213
SNP Nexus

SNPshotrs128624213
SNPdbers128624213
MSV3drs128624213
GWAS Ctlgrs128624213
Max Magnitude0
OMIM300371
Desc
Variant0001
Relatedalso
ClinVar
Risk rs128624213(A;A)
Alt rs128624213(A;A)
Reference rs128624213(G;G)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene BCAP31 ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.152991592G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012044.2,