rs776095655
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs776095655(A;A) |
Make rs776095655(A;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 42927684 |
Gene | SLC2A1 |
is a | snp |
is | mentioned by |
dbSNP | rs776095655 |
dbSNP (classic) | rs776095655 |
ClinGen | rs776095655 |
ebi | rs776095655 |
HLI | rs776095655 |
Exac | rs776095655 |
Gnomad | rs776095655 |
Varsome | rs776095655 |
LitVar | rs776095655 |
Map | rs776095655 |
PheGenI | rs776095655 |
Biobank | rs776095655 |
1000 genomes | rs776095655 |
hgdp | rs776095655 |
ensembl | rs776095655 |
geneview | rs776095655 |
scholar | rs776095655 |
rs776095655 | |
pharmgkb | rs776095655 |
gwascentral | rs776095655 |
openSNP | rs776095655 |
23andMe | rs776095655 |
SNPshot | rs776095655 |
SNPdbe | rs776095655 |
MSV3d | rs776095655 |
GWAS Ctlg | rs776095655 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776095655(A;A) rs776095655(T;T) |
Alt | rs776095655(A;A) rs776095655(T;T) |
Reference | Rs776095655(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC2A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43393355C>T |
CLNSRC | |
CLNACC | RCV000364606.1, |