rs121909738
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs121909738(A;G) |
Make rs121909738(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 42929694 |
Gene | SLC2A1 |
is a | snp |
is | mentioned by |
dbSNP | rs121909738 |
dbSNP (classic) | rs121909738 |
ClinGen | rs121909738 |
ebi | rs121909738 |
HLI | rs121909738 |
Exac | rs121909738 |
Gnomad | rs121909738 |
Varsome | rs121909738 |
LitVar | rs121909738 |
Map | rs121909738 |
PheGenI | rs121909738 |
Biobank | rs121909738 |
1000 genomes | rs121909738 |
hgdp | rs121909738 |
ensembl | rs121909738 |
geneview | rs121909738 |
scholar | rs121909738 |
rs121909738 | |
pharmgkb | rs121909738 |
gwascentral | rs121909738 |
openSNP | rs121909738 |
23andMe | rs121909738 |
SNPshot | rs121909738 |
SNPdbe | rs121909738 |
MSV3d | rs121909738 |
GWAS Ctlg | rs121909738 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909738(G;G) |
Alt | rs121909738(G;G) |
Reference | Rs121909738(A;A) |
Significance | Untested |
Disease | |
Variation | info |
Gene | SLC2A1 |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000001.10:g.43395365T>C |
CLNSRC | |
CLNACC |