PRM2, protamine 2, 5620

N. diseases: 9; N. variants: 3
Disease: Male infertility ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1646022
rs1646022 		16 11276073 intron variant C/G;T snv 0.37
CUI: C0021364
Disease: Male infertility
Male infertility 		Male Urogenital Diseases 0.020 1.000 2 2017 2018
dbSNP: rs2070923
rs2070923 		16 11275998 intron variant G/C;T snv 4.1E-06; 0.41
CUI: C0021364
Disease: Male infertility
Male infertility 		Male Urogenital Diseases 0.010 1.000 1 2015 2015
dbSNP: rs375376464
rs375376464 		16 11276355 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0021364
Disease: Male infertility
Male infertility 		Male Urogenital Diseases 0.010 1.000 1 2018 2018