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rs76715876

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
(C;T) 3 Carrier of a MMAF male infertility mutation
Make rs76715876(T;T)
is asnp
is mentioned by
dbSNPrs76715876
dbSNP (classic)rs76715876
ClinGenrs76715876
ebirs76715876
HLIrs76715876
Exacrs76715876
Gnomadrs76715876
Varsomers76715876
LitVarrs76715876
Maprs76715876
PheGenIrs76715876
Biobankrs76715876
1000 genomesrs76715876
hgdprs76715876
ensemblrs76715876
geneviewrs76715876
scholarrs76715876
googlers76715876
pharmgkbrs76715876
gwascentralrs76715876
openSNPrs76715876
23andMers76715876
SNPshotrs76715876
SNPdbers76715876
MSV3drs76715876
GWAS Ctlgrs76715876
Max Magnitude3

aka c.176+1G>A; MMAF male infertility 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.