rs1057524902
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1057524902(A;A) |
Make rs1057524902(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 44145495 |
Gene | GCK |
is a | snp |
is | mentioned by |
dbSNP | rs1057524902 |
dbSNP (classic) | rs1057524902 |
ClinGen | rs1057524902 |
ebi | rs1057524902 |
HLI | rs1057524902 |
Exac | rs1057524902 |
Gnomad | rs1057524902 |
Varsome | rs1057524902 |
LitVar | rs1057524902 |
Map | rs1057524902 |
PheGenI | rs1057524902 |
Biobank | rs1057524902 |
1000 genomes | rs1057524902 |
hgdp | rs1057524902 |
ensembl | rs1057524902 |
geneview | rs1057524902 |
scholar | rs1057524902 |
rs1057524902 | |
pharmgkb | rs1057524902 |
gwascentral | rs1057524902 |
openSNP | rs1057524902 |
23andMe | rs1057524902 |
SNPshot | rs1057524902 |
SNPdbe | rs1057524902 |
MSV3d | rs1057524902 |
GWAS Ctlg | rs1057524902 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057524902(A;A) |
Alt | rs1057524902(A;A) |
Reference | Rs1057524902(T;T) |
Significance | Pathogenic |
Disease | Monogenic diabetes |
Variation | info |
Gene | GCK |
CLNDBN | Monogenic diabetes |
Reversed | 1 |
HGVS | NC_000007.13:g.44185094A>T |
CLNSRC | |
CLNACC | RCV000445532.1, |