rs104894236
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs104894236(A;A) |
Make rs104894236(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 17388056 |
Gene | KCNJ11 |
is a | snp |
is | mentioned by |
dbSNP | rs104894236 |
dbSNP (classic) | rs104894236 |
ClinGen | rs104894236 |
ebi | rs104894236 |
HLI | rs104894236 |
Exac | rs104894236 |
Gnomad | rs104894236 |
Varsome | rs104894236 |
LitVar | rs104894236 |
Map | rs104894236 |
PheGenI | rs104894236 |
Biobank | rs104894236 |
1000 genomes | rs104894236 |
hgdp | rs104894236 |
ensembl | rs104894236 |
geneview | rs104894236 |
scholar | rs104894236 |
rs104894236 | |
pharmgkb | rs104894236 |
gwascentral | rs104894236 |
openSNP | rs104894236 |
23andMe | rs104894236 |
SNPshot | rs104894236 |
SNPdbe | rs104894236 |
MSV3d | rs104894236 |
GWAS Ctlg | rs104894236 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104894236(A;A) rs104894236(T;T) |
Alt | rs104894236(A;A) rs104894236(T;T) |
Reference | Rs104894236(C;C) |
Significance | Pathogenic |
Disease | Islet cell hyperplasia |
Variation | info |
Gene | KCNJ11 |
CLNDBN | Islet cell hyperplasia |
Reversed | 1 |
HGVS | NC_000011.9:g.17409603G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000009208.3, |