DLGAP2, DLG associated protein 2, 9228

N. diseases: 22; N. variants: 11
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: rs17669535
rs17669535 		8 1295964 intron variant C/G snv 7.4E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.800 1.000 1 2013 2013
dbSNP: rs10111688
rs10111688 		1.000 0.040 8 1310504 intron variant C/T snv 0.18
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs139288166
rs139288166 		1.000 0.080 8 755922 intron variant A/C snv 5.9E-03
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2020 2020
dbSNP: rs1393703
rs1393703 		1.000 0.080 8 832845 intron variant A/G snv 0.20
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs17062789
rs17062789 		8 1203198 intron variant G/A;C snv
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs17062789
rs17062789 		8 1203198 intron variant G/A;C snv
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement 		0.700 1.000 1 2015 2015
dbSNP: rs17062791
rs17062791 		8 1203431 intron variant C/T snv 0.14
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs17062791
rs17062791 		8 1203431 intron variant C/T snv 0.14
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement 		0.700 1.000 1 2015 2015
dbSNP: rs2404298
rs2404298 		1.000 0.080 8 1420853 intron variant A/G snv 0.84
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2404298
rs2404298 		1.000 0.080 8 1420853 intron variant A/G snv 0.84
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs28680850
rs28680850 		8 1425554 intron variant G/A snv 0.22
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2014 2014
dbSNP: rs34003842
rs34003842 		8 1206131 intron variant G/A;C;T snv
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs34003842
rs34003842 		8 1206131 intron variant G/A;C;T snv
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement 		0.700 1.000 1 2015 2015
dbSNP: rs4876094
rs4876094 		1.000 0.040 8 1309780 intron variant T/C snv 0.68
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs73670671
rs73670671 		8 1203645 intron variant T/C;G snv
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement 		0.700 1.000 1 2015 2015
dbSNP: rs73670671
rs73670671 		8 1203645 intron variant T/C;G snv
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.700 1.000 1 2015 2015