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rs193922093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs193922093(-;-)
Make rs193922093(-;C)
Make rs193922093(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153736486
GeneABCD1
is asnp
is mentioned by
dbSNPrs193922093
ebirs193922093
HLIrs193922093
Exacrs193922093
Varsomers193922093
Maprs193922093
PheGenIrs193922093
hapmaprs193922093
1000 genomesrs193922093
hgdprs193922093
ensemblrs193922093
gopubmedrs193922093
geneviewrs193922093
scholarrs193922093
googlers193922093
pharmgkbrs193922093
gwascentralrs193922093
openSNPrs193922093
23andMers193922093
23andMe allrs193922093
SNP Nexus

SNPshotrs193922093
SNPdbers193922093
MSV3drs193922093
GWAS Ctlgrs193922093
Max Magnitude0
ClinVar
Risk rs193922093(C;C)
Alt rs193922093(C;C)
Reference rs193922093(;)
Significance Probable-Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153001940dupC
CLNSRC ClinVar LabCorp
CLNACC RCV000029284.1,