rs797044781
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 7.7 | X-linked adrenoleukodystrophy; symptoms and age of onset highly variable |
(A;G) | 4.4 | Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible |
(G;G) | 0 | common in clinvar |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 153742986 |
Gene | ABCD1 |
is a | snp |
is | mentioned by |
dbSNP | rs797044781 |
dbSNP (classic) | rs797044781 |
ClinGen | rs797044781 |
ebi | rs797044781 |
HLI | rs797044781 |
Exac | rs797044781 |
Gnomad | rs797044781 |
Varsome | rs797044781 |
LitVar | rs797044781 |
Map | rs797044781 |
PheGenI | rs797044781 |
Biobank | rs797044781 |
1000 genomes | rs797044781 |
hgdp | rs797044781 |
ensembl | rs797044781 |
geneview | rs797044781 |
scholar | rs797044781 |
rs797044781 | |
pharmgkb | rs797044781 |
gwascentral | rs797044781 |
openSNP | rs797044781 |
23andMe | rs797044781 |
SNPshot | rs797044781 |
SNPdbe | rs797044781 |
MSV3d | rs797044781 |
GWAS Ctlg | rs797044781 |
Max Magnitude | 7.7 |
ClinVar | |
---|---|
Risk | Rs797044781(A;A) |
Alt | Rs797044781(A;A) |
Reference | Rs797044781(G;G) |
Significance | Pathogenic |
Disease | Adrenoleukodystrophy |
Variation | info |
Gene | ABCD1 |
CLNDBN | Adrenoleukodystrophy |
Reversed | 0 |
HGVS | NC_000023.10:g.153008440G>A |
CLNSRC | |
CLNACC | RCV000180095.1, |