rs6750998
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs6750998(A;A) |
| Make rs6750998(A;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 88583424 |
| Gene | EIF2AK3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6750998 |
| dbSNP (classic) | rs6750998 |
| ClinGen | rs6750998 |
| ebi | rs6750998 |
| HLI | rs6750998 |
| Exac | rs6750998 |
| Gnomad | rs6750998 |
| Varsome | rs6750998 |
| LitVar | rs6750998 |
| Map | rs6750998 |
| PheGenI | rs6750998 |
| Biobank | rs6750998 |
| 1000 genomes | rs6750998 |
| hgdp | rs6750998 |
| ensembl | rs6750998 |
| geneview | rs6750998 |
| scholar | rs6750998 |
| rs6750998 | |
| pharmgkb | rs6750998 |
| gwascentral | rs6750998 |
| openSNP | rs6750998 |
| 23andMe | rs6750998 |
| SNPshot | rs6750998 |
| SNPdbe | rs6750998 |
| MSV3d | rs6750998 |
| GWAS Ctlg | rs6750998 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24985580] Common variants in PERK, JNK, BIP and XBP1 genes are associated with the risk of prediabetes or diabetes-related phenotypes in a Chinese population
| ClinVar | |
|---|---|
| Risk | rs6750998(A;A) |
| Alt | rs6750998(A;A) |
| Reference | Rs6750998(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | not specified Wolcott-Rallison dysplasia |
| Variation | info |
| Gene | EIF2AK3 |
| CLNDBN | not specified Wolcott-Rallison dysplasia |
| Reversed | 0 |
| HGVS | NC_000002.11:g.88882942T>A |
| CLNSRC | ClinVar University of Chicago |
| CLNACC | RCV000116966.2, RCV000307874.1, |
