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.