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rs193922094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922094(C;C)
Make rs193922094(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153740195
GeneABCD1
is asnp
is mentioned by
dbSNPrs193922094
ebirs193922094
HLIrs193922094
Exacrs193922094
Varsomers193922094
Maprs193922094
PheGenIrs193922094
hapmaprs193922094
1000 genomesrs193922094
hgdprs193922094
ensemblrs193922094
gopubmedrs193922094
geneviewrs193922094
scholarrs193922094
googlers193922094
pharmgkbrs193922094
gwascentralrs193922094
openSNPrs193922094
23andMers193922094
23andMe allrs193922094
SNP Nexus

SNPshotrs193922094
SNPdbers193922094
MSV3drs193922094
GWAS Ctlgrs193922094
Max Magnitude0
ClinVar
Risk rs193922094(C;C)
Alt rs193922094(C;C)
Reference rs193922094(T;T)
Significance Probable-Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153005649T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029285.1,