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, |