rs1489738488
A SNP. Its most notable genotype is C;G: Carrier of a MMAF male infertility mutation
- Gene
- None listed
- Highest magnitude
- 3.0Important
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;GMost notableBadCarrier of a MMAF male infertility mutation
- G;GGoodcommon/normal
On SNPedia: (C;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
aka c.1107C>G (p.Tyr369*); MMAF recessive mutation. [note: cDNA is on reverse strand] : Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice.
C;G
Unaffected in absence of a second TTC29 gene mutation
Source and license
Adapted from rs1489738488 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.