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rs35576928

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs35576928(G;G)
Make rs35576928(G;T)
Make rs35576928(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position11281137
GenePRM1
is asnp
is mentioned by
dbSNPrs35576928
ebirs35576928
HLIrs35576928
Exacrs35576928
Varsomers35576928
Maprs35576928
PheGenIrs35576928
hapmaprs35576928
1000 genomesrs35576928
hgdprs35576928
ensemblrs35576928
gopubmedrs35576928
geneviewrs35576928
scholarrs35576928
googlers35576928
pharmgkbrs35576928
gwascentralrs35576928
openSNPrs35576928
23andMers35576928
23andMe allrs35576928
SNP Nexus

SNPshotrs35576928
SNPdbers35576928
MSV3drs35576928
GWAS Ctlgrs35576928
GMAF0.005051
Max Magnitude0
Also known as c.102G>T transversion that results in an p.Arg34Ser amino acid.


[PMID 23079002] PRM1 variant rs35576928 (Arg>Ser) is associated with defective spermatogenesis in the Chinese Han population

[PMID 18381856] Low-frequency protamine 1 gene transversions c.102G->T and c.-107G->C do not correlate with male infertility

[PMID 17494104] Mutations in the protamine 1 gene associated with male infertility

Male Infertility


[PMID 26472740OA-icon.png] Polymorphisms in Protamine 1 and Protamine 2 predict the risk of male infertility: a meta-analysis