rs188541504, THEG

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Male infertility
CUI: C0021364
Disease: Male infertility
0.030 GeneticVariation BEFREE But, there was a significant association between 368A>G and male</span> infertility</span>. 29453813 2018
Male infertility
CUI: C0021364
Disease: Male infertility
0.030 GeneticVariation BEFREE It is concluded that H2BFWT gene c.-9C>T and c.368A>G polymorphisms might be genetic risk factors for idiopathic male infertility. 28370107 2018
Male infertility
CUI: C0021364
Disease: Male infertility
0.030 GeneticVariation BEFREE These results indicated that the polymorphism -9C>T and 368A>G in H2BFWT gene are associated with male infertility with idiopathic azoospermia or oligozoospermia, suggesting that H2BFWT gene might be contribute to susceptibility to spermatogenesis impairment in Chinese population. 22509975 2012
Oligospermia
CUI: C0028960
Disease: Oligospermia
0.010 GeneticVariation BEFREE These results indicated that the polymorphism -9C>T and 368A>G in H2BFWT gene are associated with male infertility with idiopathic azoospermia or oligozoospermia, suggesting that H2BFWT gene might be contribute to susceptibility to spermatogenesis impairment in Chinese population. 22509975 2012
Azoospermia
CUI: C0004509
Disease: Azoospermia
0.010 GeneticVariation BEFREE These results indicated that the polymorphism -9C>T and 368A>G in H2BFWT gene are associated with male infertility with idiopathic azoospermia or oligozoospermia, suggesting that H2BFWT gene might be contribute to susceptibility to spermatogenesis impairment in Chinese population. 22509975 2012