rs988213
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs988213(A;A) |
| Make rs988213(A;G) |
| Make rs988213(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 46545004 |
| Gene | LOXHD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs988213 |
| dbSNP (classic) | rs988213 |
| ClinGen | rs988213 |
| ebi | rs988213 |
| HLI | rs988213 |
| Exac | rs988213 |
| Gnomad | rs988213 |
| Varsome | rs988213 |
| LitVar | rs988213 |
| Map | rs988213 |
| PheGenI | rs988213 |
| Biobank | rs988213 |
| 1000 genomes | rs988213 |
| hgdp | rs988213 |
| ensembl | rs988213 |
| geneview | rs988213 |
| scholar | rs988213 |
| rs988213 | |
| pharmgkb | rs988213 |
| gwascentral | rs988213 |
| openSNP | rs988213 |
| 23andMe | rs988213 |
| SNPshot | rs988213 |
| SNPdbe | rs988213 |
| MSV3d | rs988213 |
| GWAS Ctlg | rs988213 |
| GMAF | 0.3714 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients.[PMID 17671248]
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 18
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
