rs16853834
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16853834(C;C) |
| Make rs16853834(C;T) |
| Make rs16853834(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 215345513 |
| Gene | ATIC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16853834 |
| dbSNP (classic) | rs16853834 |
| ClinGen | rs16853834 |
| ebi | rs16853834 |
| HLI | rs16853834 |
| Exac | rs16853834 |
| Gnomad | rs16853834 |
| Varsome | rs16853834 |
| LitVar | rs16853834 |
| Map | rs16853834 |
| PheGenI | rs16853834 |
| Biobank | rs16853834 |
| 1000 genomes | rs16853834 |
| hgdp | rs16853834 |
| ensembl | rs16853834 |
| geneview | rs16853834 |
| scholar | rs16853834 |
| rs16853834 | |
| pharmgkb | rs16853834 |
| gwascentral | rs16853834 |
| openSNP | rs16853834 |
| 23andMe | rs16853834 |
| SNPshot | rs16853834 |
| SNPdbe | rs16853834 |
| MSV3d | rs16853834 |
| GWAS Ctlg | rs16853834 |
| GMAF | 0.168 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22461784
] Regular Multivitamin Supplement Use, Single Nucleotide Polymorphisms in ATIC, SHMT2, and SLC46A1, and Risk of Ovarian Carcinoma
[PMID 17847007] Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.
[PMID 22450926] Genetic polymorphisms in key methotrexate pathway genes are associated with response to treatment in rheumatoid arthritis patients.
