rs749426767
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs749426767(C;T) |
Make rs749426767(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 42929215 |
Gene | SLC2A1 |
is a | snp |
is | mentioned by |
dbSNP | rs749426767 |
dbSNP (classic) | rs749426767 |
ClinGen | rs749426767 |
ebi | rs749426767 |
HLI | rs749426767 |
Exac | rs749426767 |
Gnomad | rs749426767 |
Varsome | rs749426767 |
LitVar | rs749426767 |
Map | rs749426767 |
PheGenI | rs749426767 |
Biobank | rs749426767 |
1000 genomes | rs749426767 |
hgdp | rs749426767 |
ensembl | rs749426767 |
geneview | rs749426767 |
scholar | rs749426767 |
rs749426767 | |
pharmgkb | rs749426767 |
gwascentral | rs749426767 |
openSNP | rs749426767 |
23andMe | rs749426767 |
SNPshot | rs749426767 |
SNPdbe | rs749426767 |
MSV3d | rs749426767 |
GWAS Ctlg | rs749426767 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs749426767(T;T) |
Alt | rs749426767(T;T) |
Reference | Rs749426767(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC2A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43394886C>T |
CLNSRC | |
CLNACC | RCV000439467.1, |