rs570388861
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs570388861(A;A) |
Make rs570388861(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 17408415 |
Gene | ABCC8 |
is a | snp |
is | mentioned by |
dbSNP | rs570388861 |
dbSNP (classic) | rs570388861 |
ClinGen | rs570388861 |
ebi | rs570388861 |
HLI | rs570388861 |
Exac | rs570388861 |
Gnomad | rs570388861 |
Varsome | rs570388861 |
LitVar | rs570388861 |
Map | rs570388861 |
PheGenI | rs570388861 |
Biobank | rs570388861 |
1000 genomes | rs570388861 |
hgdp | rs570388861 |
ensembl | rs570388861 |
geneview | rs570388861 |
scholar | rs570388861 |
rs570388861 | |
pharmgkb | rs570388861 |
gwascentral | rs570388861 |
openSNP | rs570388861 |
23andMe | rs570388861 |
SNPshot | rs570388861 |
SNPdbe | rs570388861 |
MSV3d | rs570388861 |
GWAS Ctlg | rs570388861 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs570388861(A;A) rs570388861(C;C) |
Alt | rs570388861(A;A) rs570388861(C;C) |
Reference | Rs570388861(G;G) |
Significance | Pathogenic |
Disease | Persistent hyperinsulinemic hypoglycemia of infancy not provided |
Variation | info |
Gene | ABCC8 |
CLNDBN | Persistent hyperinsulinemic hypoglycemia of infancy not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.17429962G>A |
CLNSRC | Counsyl |
CLNACC | RCV000169216.1, RCV000201910.1, |