rs74339576
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
(G;G) | 0 | common in clinvar |
Make rs74339576(A;A) |
Make rs74339576(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 17387190 |
Gene | KCNJ11 |
is a | snp |
is | mentioned by |
dbSNP | rs74339576 |
dbSNP (classic) | rs74339576 |
ClinGen | rs74339576 |
ebi | rs74339576 |
HLI | rs74339576 |
Exac | rs74339576 |
Gnomad | rs74339576 |
Varsome | rs74339576 |
LitVar | rs74339576 |
Map | rs74339576 |
PheGenI | rs74339576 |
Biobank | rs74339576 |
1000 genomes | rs74339576 |
hgdp | rs74339576 |
ensembl | rs74339576 |
geneview | rs74339576 |
scholar | rs74339576 |
rs74339576 | |
pharmgkb | rs74339576 |
gwascentral | rs74339576 |
openSNP | rs74339576 |
23andMe | rs74339576 |
SNPshot | rs74339576 |
SNPdbe | rs74339576 |
MSV3d | rs74339576 |
GWAS Ctlg | rs74339576 |
GMAF | 0.0004591 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs74339576(A;A) rs74339576(T;T) |
Alt | rs74339576(A;A) rs74339576(T;T) |
Reference | Rs74339576(G;G) |
Significance | Pathogenic |
Disease | Islet cell hyperplasia |
Variation | info |
Gene | KCNJ11 |
CLNDBN | Islet cell hyperplasia |
Reversed | 1 |
HGVS | NC_000011.9:g.17408737C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000009220.2, |