rs763399136
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common/normal |
(G;T) | 3 | Carrier of a MMAF male infertility mutation |
Make rs763399136(T;T) |
is a | snp |
is | mentioned by |
dbSNP | rs763399136 |
dbSNP (classic) | rs763399136 |
ClinGen | rs763399136 |
ebi | rs763399136 |
HLI | rs763399136 |
Exac | rs763399136 |
Gnomad | rs763399136 |
Varsome | rs763399136 |
LitVar | rs763399136 |
Map | rs763399136 |
PheGenI | rs763399136 |
Biobank | rs763399136 |
1000 genomes | rs763399136 |
hgdp | rs763399136 |
ensembl | rs763399136 |
geneview | rs763399136 |
scholar | rs763399136 |
rs763399136 | |
pharmgkb | rs763399136 |
gwascentral | rs763399136 |
openSNP | rs763399136 |
23andMe | rs763399136 |
SNPshot | rs763399136 |
SNPdbe | rs763399136 |
MSV3d | rs763399136 |
GWAS Ctlg | rs763399136 |
Max Magnitude | 3 |
aka c.750C>A; MMAF recessive mutation. [note: cDNA is on reverse strand]
[PMID 31735292]: Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.