rs771386274
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs771386274(C;T) |
Make rs771386274(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 42929868 |
Gene | SLC2A1 |
is a | snp |
is | mentioned by |
dbSNP | rs771386274 |
dbSNP (classic) | rs771386274 |
ClinGen | rs771386274 |
ebi | rs771386274 |
HLI | rs771386274 |
Exac | rs771386274 |
Gnomad | rs771386274 |
Varsome | rs771386274 |
LitVar | rs771386274 |
Map | rs771386274 |
PheGenI | rs771386274 |
Biobank | rs771386274 |
1000 genomes | rs771386274 |
hgdp | rs771386274 |
ensembl | rs771386274 |
geneview | rs771386274 |
scholar | rs771386274 |
rs771386274 | |
pharmgkb | rs771386274 |
gwascentral | rs771386274 |
openSNP | rs771386274 |
23andMe | rs771386274 |
SNPshot | rs771386274 |
SNPdbe | rs771386274 |
MSV3d | rs771386274 |
GWAS Ctlg | rs771386274 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs771386274(A;A) rs771386274(T;T) |
Alt | rs771386274(A;A) rs771386274(T;T) |
Reference | Rs771386274(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC2A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43395539C>A |
CLNSRC | |
CLNACC | RCV000254738.1, |