rs2477686, PLCH2

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Non-obstructive azoospermia
CUI: C4021107
Disease: Non-obstructive azoospermia
88 0.807 0.040 1 2461209 intron variant G/C snv 0.64 0.720 1.000 2 2011 2015
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.807 0.040 1 2461209 intron variant G/C snv 0.64 0.700 1.000 1 2011 2011
Azoospermia, Nonobstructive
CUI: C1847540
Disease: Azoospermia, Nonobstructive
22 0.807 0.040 1 2461209 intron variant G/C snv 0.64 0.020 0.500 2 2014 2019
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.807 0.040 1 2461209 intron variant G/C snv 0.64 0.020 0.500 2 2014 2019
Asthenozoospermia
CUI: C0403823
Disease: Asthenozoospermia
17 0.807 0.040 1 2461209 intron variant G/C snv 0.64 0.010 1.000 1 2018 2018
Oligoasthenozoospermia
CUI: C3164407
Disease: Oligoasthenozoospermia
6 0.807 0.040 1 2461209 intron variant G/C snv 0.64 0.010 1.000 1 2018 2018
Oligospermia
CUI: C0028960
Disease: Oligospermia
72 0.807 0.040 1 2461209 intron variant G/C snv 0.64 0.010 1 2019 2019