H2BW1, H2B.W histone 1, 158983

N. diseases: 3; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs553509
rs553509
Entrez Id: 158983
Gene Symbol: H2BW1
H2BW1
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
dbSNP: rs553509
rs553509
Entrez Id: 158983
Gene Symbol: H2BW1
H2BW1
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
dbSNP: rs553509
rs553509
Entrez Id: 158983
Gene Symbol: H2BW1
H2BW1
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
dbSNP: rs553509
rs553509
Entrez Id: 158983
Gene Symbol: H2BW1
H2BW1
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
dbSNP: rs553509
rs553509
Entrez Id: 158983
Gene Symbol: H2BW1
H2BW1
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