DAZL, deleted in azoospermia like, 1618

N. diseases: 14; N. variants: 4
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: rs12494691
rs12494691 		3 16658827 intron variant G/A;C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs6787063
rs6787063 		3 16594958 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs121918346
rs121918346 		0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06
CUI: C4016734
Disease: SPERMATOGENIC FAILURE, SUSCEPTIBILITY TO
SPERMATOGENIC FAILURE, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs121918346
rs121918346 		0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06
CUI: C0028960
Disease: Oligospermia
Oligospermia 		Male Urogenital Diseases 0.020 0.500 2 2002 2005
dbSNP: rs11710967
rs11710967 		3 16598568 missense variant T/A;C snv 0.11
CUI: C0021364
Disease: Male infertility
Male infertility 		Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs121918346
rs121918346 		0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06
CUI: C1384583
Disease: Congenital absence of germinal epithelium of testes
Congenital absence of germinal epithelium of testes 		Male Urogenital Diseases 0.010 1.000 1 2002 2002
dbSNP: rs121918346
rs121918346 		0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06
CUI: C0004509
Disease: Azoospermia
Azoospermia 		Male Urogenital Diseases 0.010 < 0.001 1 2005 2005
dbSNP: rs121918346
rs121918346 		0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06
CUI: C0021364
Disease: Male infertility
Male infertility 		Male Urogenital Diseases 0.010 1.000 1 2014 2014