rs193922399
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs193922399(G;G) |
Make rs193922399(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 17404527 |
Gene | ABCC8 |
is a | snp |
is | mentioned by |
dbSNP | rs193922399 |
dbSNP (classic) | rs193922399 |
ClinGen | rs193922399 |
ebi | rs193922399 |
HLI | rs193922399 |
Exac | rs193922399 |
Gnomad | rs193922399 |
Varsome | rs193922399 |
LitVar | rs193922399 |
Map | rs193922399 |
PheGenI | rs193922399 |
Biobank | rs193922399 |
1000 genomes | rs193922399 |
hgdp | rs193922399 |
ensembl | rs193922399 |
geneview | rs193922399 |
scholar | rs193922399 |
rs193922399 | |
pharmgkb | rs193922399 |
gwascentral | rs193922399 |
openSNP | rs193922399 |
23andMe | rs193922399 |
SNPshot | rs193922399 |
SNPdbe | rs193922399 |
MSV3d | rs193922399 |
GWAS Ctlg | rs193922399 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs193922399(G;G) |
Alt | rs193922399(G;G) |
Reference | Rs193922399(T;T) |
Significance | Probable-Pathogenic |
Disease | Neonatal diabetes mellitus |
Variation | info |
Gene | ABCC8 |
CLNDBN | Neonatal diabetes mellitus |
Reversed | 1 |
HGVS | NC_000011.9:g.17426074A>C |
CLNSRC | ClinVar LabCorp |
CLNACC | RCV000029256.1, |