rs1063635
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs1063635(A;A) |
| Make rs1063635(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31412154 |
| Gene | MICA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1063635 |
| dbSNP (classic) | rs1063635 |
| ClinGen | rs1063635 |
| ebi | rs1063635 |
| HLI | rs1063635 |
| Exac | rs1063635 |
| Gnomad | rs1063635 |
| Varsome | rs1063635 |
| LitVar | rs1063635 |
| Map | rs1063635 |
| PheGenI | rs1063635 |
| Biobank | rs1063635 |
| 1000 genomes | rs1063635 |
| hgdp | rs1063635 |
| ensembl | rs1063635 |
| geneview | rs1063635 |
| scholar | rs1063635 |
| rs1063635 | |
| pharmgkb | rs1063635 |
| gwascentral | rs1063635 |
| openSNP | rs1063635 |
| 23andMe | rs1063635 |
| SNPshot | rs1063635 |
| SNPdbe | rs1063635 |
| MSV3d | rs1063635 |
| GWAS Ctlg | rs1063635 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21653640] |
| Trait | |
| Title | Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways. |
| Risk Allele | |
| P-val | 1E-17 |
| Odds Ratio | 1.3500 [1.27-1.45] |
[PMID 20018019
] Two-stage joint selection method to identify candidate markers from genome-wide association studies.
[PMID 20041220] Autoimmune disease classification by inverse association with SNP alleles.
| ClinVar | |
|---|---|
| Risk | rs1063635(A;A) |
| Alt | rs1063635(A;A) |
| Reference | Rs1063635(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | MICA |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000006.11:g.31379931G>A |
| CLNSRC | |
| CLNACC | RCV000455790.1, |
