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rs763399136

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common/normal
(G;T) 3 Carrier of a MMAF male infertility mutation
Make rs763399136(T;T)
is asnp
is mentioned by
dbSNPrs763399136
dbSNP (classic)rs763399136
ClinGenrs763399136
ebirs763399136
HLIrs763399136
Exacrs763399136
Gnomadrs763399136
Varsomers763399136
LitVarrs763399136
Maprs763399136
PheGenIrs763399136
Biobankrs763399136
1000 genomesrs763399136
hgdprs763399136
ensemblrs763399136
geneviewrs763399136
scholarrs763399136
googlers763399136
pharmgkbrs763399136
gwascentralrs763399136
openSNPrs763399136
23andMers763399136
SNPshotrs763399136
SNPdbers763399136
MSV3drs763399136
GWAS Ctlgrs763399136
Max Magnitude3

aka c.750C>A; MMAF recessive mutation. [note: cDNA is on reverse strand]

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