rs76715876
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | 3 | Carrier of a MMAF male infertility mutation |
Make rs76715876(T;T) |
is a | snp |
is | mentioned by |
dbSNP | rs76715876 |
dbSNP (classic) | rs76715876 |
ClinGen | rs76715876 |
ebi | rs76715876 |
HLI | rs76715876 |
Exac | rs76715876 |
Gnomad | rs76715876 |
Varsome | rs76715876 |
LitVar | rs76715876 |
Map | rs76715876 |
PheGenI | rs76715876 |
Biobank | rs76715876 |
1000 genomes | rs76715876 |
hgdp | rs76715876 |
ensembl | rs76715876 |
geneview | rs76715876 |
scholar | rs76715876 |
rs76715876 | |
pharmgkb | rs76715876 |
gwascentral | rs76715876 |
openSNP | rs76715876 |
23andMe | rs76715876 |
SNPshot | rs76715876 |
SNPdbe | rs76715876 |
MSV3d | rs76715876 |
GWAS Ctlg | rs76715876 |
Max Magnitude | 3 |
aka c.176+1G>A; MMAF male infertility 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.