rs587780346
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs587780346(A;C) |
Make rs587780346(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 7 |
Position | 44149823 |
Gene | GCK, LOC105375258 |
is a | snp |
is | mentioned by |
dbSNP | rs587780346 |
dbSNP (classic) | rs587780346 |
ClinGen | rs587780346 |
ebi | rs587780346 |
HLI | rs587780346 |
Exac | rs587780346 |
Gnomad | rs587780346 |
Varsome | rs587780346 |
LitVar | rs587780346 |
Map | rs587780346 |
PheGenI | rs587780346 |
Biobank | rs587780346 |
1000 genomes | rs587780346 |
hgdp | rs587780346 |
ensembl | rs587780346 |
geneview | rs587780346 |
scholar | rs587780346 |
rs587780346 | |
pharmgkb | rs587780346 |
gwascentral | rs587780346 |
openSNP | rs587780346 |
23andMe | rs587780346 |
SNPshot | rs587780346 |
SNPdbe | rs587780346 |
MSV3d | rs587780346 |
GWAS Ctlg | rs587780346 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780346(C;C) |
Alt | rs587780346(C;C) |
Reference | Rs587780346(A;A) |
Significance | Probable-Pathogenic |
Disease | Diabetes mellitus |
Variation | info |
Gene | GCK |
CLNDBN | Diabetes mellitus, gestational |
Reversed | 1 |
HGVS | NC_000007.13:g.44189422T>G |
CLNSRC | |
CLNACC | RCV000117132.1, |