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rs128624218

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs128624218(A;A)
Make rs128624218(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153726062
GeneABCD1, BCAP31
is asnp
is mentioned by
dbSNPrs128624218
ebirs128624218
HLIrs128624218
Exacrs128624218
Varsomers128624218
Maprs128624218
PheGenIrs128624218
hapmaprs128624218
1000 genomesrs128624218
hgdprs128624218
ensemblrs128624218
gopubmedrs128624218
geneviewrs128624218
scholarrs128624218
googlers128624218
pharmgkbrs128624218
gwascentralrs128624218
openSNPrs128624218
23andMers128624218
23andMe allrs128624218
SNP Nexus

SNPshotrs128624218
SNPdbers128624218
MSV3drs128624218
GWAS Ctlgrs128624218
Max Magnitude0
OMIM300371
Desc
Variant0008
Relatedalso
ClinVar
Risk rs128624218(A;A)
Alt rs128624218(A;A)
Reference rs128624218(G;G)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene BCAP31 ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.152991517G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012051.17,