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rs11146842

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11146842(A;A)
Make rs11146842(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153743056
GeneABCD1
is asnp
is mentioned by
dbSNPrs11146842
ebirs11146842
HLIrs11146842
Exacrs11146842
Varsomers11146842
Maprs11146842
PheGenIrs11146842
hapmaprs11146842
1000 genomesrs11146842
hgdprs11146842
ensemblrs11146842
gopubmedrs11146842
geneviewrs11146842
scholarrs11146842
googlers11146842
pharmgkbrs11146842
gwascentralrs11146842
openSNPrs11146842
23andMers11146842
23andMe allrs11146842
SNP Nexus

SNPshotrs11146842
SNPdbers11146842
MSV3drs11146842
GWAS Ctlgrs11146842
Max Magnitude0
OMIM300371
Desc
Variant0021
Relatedalso
ClinVar
Risk rs11146842(A;A)
Alt rs11146842(A;A)
Reference rs11146842(G;G)
Significance Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153008510G>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000012064.19,