rs145073701
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 7.7 | X-linked adrenoleukodystrophy; symptoms and age of onset highly variable |
(A;C) | 4.4 | Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible |
(C;C) | 0 | common/normal |
Make rs145073701(C;T) |
Make rs145073701(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 153740184 |
Gene | ABCD1 |
is a | snp |
is | mentioned by |
dbSNP | rs145073701 |
dbSNP (classic) | rs145073701 |
ClinGen | rs145073701 |
ebi | rs145073701 |
HLI | rs145073701 |
Exac | rs145073701 |
Gnomad | rs145073701 |
Varsome | rs145073701 |
LitVar | rs145073701 |
Map | rs145073701 |
PheGenI | rs145073701 |
Biobank | rs145073701 |
1000 genomes | rs145073701 |
hgdp | rs145073701 |
ensembl | rs145073701 |
geneview | rs145073701 |
scholar | rs145073701 |
rs145073701 | |
pharmgkb | rs145073701 |
gwascentral | rs145073701 |
openSNP | rs145073701 |
23andMe | rs145073701 |
SNPshot | rs145073701 |
SNPdbe | rs145073701 |
MSV3d | rs145073701 |
GWAS Ctlg | rs145073701 |
Max Magnitude | 7.7 |