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rs398123111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123111(C;T)
Make rs398123111(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153725672
GeneABCD1, BCAP31
is asnp
is mentioned by
dbSNPrs398123111
ebirs398123111
HLIrs398123111
Exacrs398123111
Varsomers398123111
Maprs398123111
PheGenIrs398123111
hapmaprs398123111
1000 genomesrs398123111
hgdprs398123111
ensemblrs398123111
gopubmedrs398123111
geneviewrs398123111
scholarrs398123111
googlers398123111
pharmgkbrs398123111
gwascentralrs398123111
openSNPrs398123111
23andMers398123111
23andMe allrs398123111
SNP Nexus

SNPshotrs398123111
SNPdbers398123111
MSV3drs398123111
GWAS Ctlgrs398123111
Max Magnitude0
ClinVar
Risk rs398123111(T;T)
Alt rs398123111(T;T)
Reference rs398123111(C;C)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene BCAP31 ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.152991127C>T
CLNSRC ClinVar Emory University
CLNACC RCV000077964.4,