rs121918346, DAZL

N. diseases: 5
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.
SPERMATOGENIC FAILURE, SUSCEPTIBILITY TO
CUI: C4016734
Disease: SPERMATOGENIC FAILURE, SUSCEPTIBILITY TO
1 0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06 0.700 0
Oligospermia
CUI: C0028960
Disease: Oligospermia
72 0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06 0.020 0.500 2 2002 2005
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06 0.010 1 2005 2005
Congenital absence of germinal epithelium of testes
CUI: C1384583
Disease: Congenital absence of germinal epithelium of testes
6 0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2002 2002
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2014 2014