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rs141446687

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 7.7 X-linked adrenoleukodystrophy; symptoms and age of onset highly variable
(A;C) 3 Carrier of X-linked adrenoleukodystrophy mutation; probably unaffected
(C;C) 0 common/normal
Make rs141446687(C;G)
Make rs141446687(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position153737191
GeneABCD1
is asnp
is mentioned by
dbSNPrs141446687
dbSNP (old)rs141446687
ClinGenrs141446687
ebirs141446687
HLIrs141446687
Exacrs141446687
Gnomadrs141446687
Varsomers141446687
Maprs141446687
PheGenIrs141446687
Biobankrs141446687
1000 genomesrs141446687
hgdprs141446687
ensemblrs141446687
gopubmedrs141446687
geneviewrs141446687
scholarrs141446687
googlers141446687
pharmgkbrs141446687
gwascentralrs141446687
openSNPrs141446687
23andMers141446687
23andMe allrs141446687
SNPshotrs141446687
SNPdbers141446687
MSV3drs141446687
GWAS Ctlgrs141446687
Max Magnitude7.7