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rs398123104

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123104(A;A)
Make rs398123104(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153740599
GeneABCD1
is asnp
is mentioned by
dbSNPrs398123104
ebirs398123104
HLIrs398123104
Exacrs398123104
Varsomers398123104
Maprs398123104
PheGenIrs398123104
hapmaprs398123104
1000 genomesrs398123104
hgdprs398123104
ensemblrs398123104
gopubmedrs398123104
geneviewrs398123104
scholarrs398123104
googlers398123104
pharmgkbrs398123104
gwascentralrs398123104
openSNPrs398123104
23andMers398123104
23andMe allrs398123104
SNP Nexus

SNPshotrs398123104
SNPdbers398123104
MSV3drs398123104
GWAS Ctlgrs398123104
Max Magnitude0
ClinVar
Risk rs398123104(A,T;A,T)
Alt rs398123104(A,T;A,T)
Reference rs398123104(C;C)
Significance Probable-Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153006053C>A
CLNSRC ClinVar Emory University
CLNACC RCV000077957.4,