rs766352190
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;CCTCC) | 3 | Carrier of a MMAF male infertility mutation |
| (CCTCCC;CCTCC) | 0 | common/normal |
| Make rs766352190(-;-) |
| is a | snp |
| is | mentioned by |
| dbSNP | rs766352190 |
| dbSNP (classic) | rs766352190 |
| ClinGen | rs766352190 |
| ebi | rs766352190 |
| HLI | rs766352190 |
| Exac | rs766352190 |
| Gnomad | rs766352190 |
| Varsome | rs766352190 |
| LitVar | rs766352190 |
| Map | rs766352190 |
| PheGenI | rs766352190 |
| Biobank | rs766352190 |
| 1000 genomes | rs766352190 |
| hgdp | rs766352190 |
| ensembl | rs766352190 |
| geneview | rs766352190 |
| scholar | rs766352190 |
| rs766352190 | |
| pharmgkb | rs766352190 |
| gwascentral | rs766352190 |
| openSNP | rs766352190 |
| 23andMe | rs766352190 |
| SNPshot | rs766352190 |
| SNPdbe | rs766352190 |
| MSV3d | rs766352190 |
| GWAS Ctlg | rs766352190 |
| Max Magnitude | 3 |
aka c.330_334delGGAGG; MMAF recessive mutation.
[PMID 31735292
]: Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.
