rs201114595
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | 4.4 | Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible |
(T;T) | 7.7 | X-linked adrenoleukodystrophy; symptoms and age of onset highly variable |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 153740638 |
Gene | ABCD1 |
is a | snp |
is | mentioned by |
dbSNP | rs201114595 |
dbSNP (classic) | rs201114595 |
ClinGen | rs201114595 |
ebi | rs201114595 |
HLI | rs201114595 |
Exac | rs201114595 |
Gnomad | rs201114595 |
Varsome | rs201114595 |
LitVar | rs201114595 |
Map | rs201114595 |
PheGenI | rs201114595 |
Biobank | rs201114595 |
1000 genomes | rs201114595 |
hgdp | rs201114595 |
ensembl | rs201114595 |
geneview | rs201114595 |
scholar | rs201114595 |
rs201114595 | |
pharmgkb | rs201114595 |
gwascentral | rs201114595 |
openSNP | rs201114595 |
23andMe | rs201114595 |
SNPshot | rs201114595 |
SNPdbe | rs201114595 |
MSV3d | rs201114595 |
GWAS Ctlg | rs201114595 |
Max Magnitude | 7.7 |