rs139722450
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs139722450(C;G) |
Make rs139722450(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 42927627 |
Gene | SLC2A1 |
is a | snp |
is | mentioned by |
dbSNP | rs139722450 |
dbSNP (classic) | rs139722450 |
ClinGen | rs139722450 |
ebi | rs139722450 |
HLI | rs139722450 |
Exac | rs139722450 |
Gnomad | rs139722450 |
Varsome | rs139722450 |
LitVar | rs139722450 |
Map | rs139722450 |
PheGenI | rs139722450 |
Biobank | rs139722450 |
1000 genomes | rs139722450 |
hgdp | rs139722450 |
ensembl | rs139722450 |
geneview | rs139722450 |
scholar | rs139722450 |
rs139722450 | |
pharmgkb | rs139722450 |
gwascentral | rs139722450 |
openSNP | rs139722450 |
23andMe | rs139722450 |
SNPshot | rs139722450 |
SNPdbe | rs139722450 |
MSV3d | rs139722450 |
GWAS Ctlg | rs139722450 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139722450(A;A) rs139722450(G;G) |
Alt | rs139722450(A;A) rs139722450(G;G) |
Reference | Rs139722450(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC2A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43393298C>A |
CLNSRC | |
CLNACC | RCV000413602.1, |