rs139582106
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs139582106(A;A) |
Make rs139582106(A;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 114684278 |
Gene | AMPD1 |
is a | snp |
is | mentioned by |
dbSNP | rs139582106 |
dbSNP (classic) | rs139582106 |
ClinGen | rs139582106 |
ebi | rs139582106 |
HLI | rs139582106 |
Exac | rs139582106 |
Gnomad | rs139582106 |
Varsome | rs139582106 |
LitVar | rs139582106 |
Map | rs139582106 |
PheGenI | rs139582106 |
Biobank | rs139582106 |
1000 genomes | rs139582106 |
hgdp | rs139582106 |
ensembl | rs139582106 |
geneview | rs139582106 |
scholar | rs139582106 |
rs139582106 | |
pharmgkb | rs139582106 |
gwascentral | rs139582106 |
openSNP | rs139582106 |
23andMe | rs139582106 |
SNPshot | rs139582106 |
SNPdbe | rs139582106 |
MSV3d | rs139582106 |
GWAS Ctlg | rs139582106 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139582106(A;A) |
Alt | rs139582106(A;A) |
Reference | Rs139582106(C;C) |
Significance | Probable-Pathogenic |
Disease | Muscle AMP deaminase deficiency not provided |
Variation | info |
Gene | AMPD1 |
CLNDBN | Muscle AMP deaminase deficiency not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.115226899C>A |
CLNSRC | |
CLNACC | RCV000178704.1, RCV000443504.1, |