Have questions? Visit https://www.reddit.com/r/SNPedia

rs766352190

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;CCTCC) 3 Carrier of a MMAF male infertility mutation
(CCTCCC;CCTCC) 0 common/normal


Make rs766352190(-;-)
is asnp
is mentioned by
dbSNPrs766352190
dbSNP (classic)rs766352190
ClinGenrs766352190
ebirs766352190
HLIrs766352190
Exacrs766352190
Gnomadrs766352190
Varsomers766352190
LitVarrs766352190
Maprs766352190
PheGenIrs766352190
Biobankrs766352190
1000 genomesrs766352190
hgdprs766352190
ensemblrs766352190
geneviewrs766352190
scholarrs766352190
googlers766352190
pharmgkbrs766352190
gwascentralrs766352190
openSNPrs766352190
23andMers766352190
SNPshotrs766352190
SNPdbers766352190
MSV3drs766352190
GWAS Ctlgrs766352190
Max Magnitude3

aka c.330_334delGGAGG; MMAF recessive mutation.

[PMID 31735292OA-icon.png]: Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.