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rs387906494

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs387906494(-;-)
Make rs387906494(-;AG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153737178
GeneABCD1
is asnp
is mentioned by
dbSNPrs387906494
ebirs387906494
HLIrs387906494
Exacrs387906494
Varsomers387906494
Maprs387906494
PheGenIrs387906494
hapmaprs387906494
1000 genomesrs387906494
hgdprs387906494
ensemblrs387906494
gopubmedrs387906494
geneviewrs387906494
scholarrs387906494
googlers387906494
pharmgkbrs387906494
gwascentralrs387906494
openSNPrs387906494
23andMers387906494
23andMe allrs387906494
SNP Nexus

SNPshotrs387906494
SNPdbers387906494
MSV3drs387906494
GWAS Ctlgrs387906494
Max Magnitude0
ClinVar
Risk rs387906494(;)
Alt rs387906494(;)
Reference rs387906494(AG;AG)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153002632_153002633delAG
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000012055.19,