PRKD1, protein kinase D1, 5587

N. diseases: 171; N. variants: 19
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: rs11847697
rs11847697
14 30045906 intron variant C/T snv 0.13
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2010 2018
dbSNP: rs2068012
rs2068012
1.000 0.040 14 29721110 intron variant T/C snv 0.28
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 4 2014 2019
dbSNP: rs11847697
rs11847697
14 30045906 intron variant C/T snv 0.13
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 2 2010 2013
dbSNP: rs11847697
rs11847697
14 30045906 intron variant C/T snv 0.13
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 2 2010 2013
dbSNP: rs971681
rs971681
14 29605481 intron variant C/T snv 0.43
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs10136330
rs10136330
14 30045129 intron variant C/T snv 9.3E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs10151686
rs10151686
14 29997260 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs11847697
rs11847697
14 30045906 intron variant C/T snv 0.13
CUI: C0455829
Disease: Waist Circumference
Waist Circumference
0.700 1.000 1 2017 2017
dbSNP: rs11847697
rs11847697
14 30045906 intron variant C/T snv 0.13
CUI: C0005910
Disease: Body Weight
Body Weight
Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2017 2017
dbSNP: rs1191600
rs1191600
14 29632435 intron variant C/A snv 0.45
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs12589992
rs12589992
14 29918314 intron variant C/T snv 6.9E-02
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2012 2012
dbSNP: rs17115145
rs17115145
14 29653203 intron variant C/T snv 0.43
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs1959440
rs1959440
1.000 0.040 14 29739424 intron variant G/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1959440
rs1959440
1.000 0.040 14 29739424 intron variant G/A;T snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2068012
rs2068012
1.000 0.040 14 29721110 intron variant T/C snv 0.28
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs225848
rs225848
1.000 0.040 14 30125451 intron variant G/A snv 0.91
CUI: C3714744
Disease: Psychosexual dysfunction
Psychosexual dysfunction
Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs225848
rs225848
1.000 0.040 14 30125451 intron variant G/A snv 0.91
CUI: C0549622
Disease: Sexual Dysfunction
Sexual Dysfunction
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Mental Disorders; Behavior and Behavior Mechanisms 0.700 1.000 1 2012 2012
dbSNP: rs2333604
rs2333604
14 29602532 intron variant C/A;T snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs28645341
rs28645341
14 29704872 intron variant T/C snv 0.32
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs55906749
rs55906749
14 30000498 intron variant T/C snv 8.1E-02
CUI: C0562350
Disease: Hip circumference
Hip circumference
0.700 1.000 1 2017 2017
dbSNP: rs61980001
rs61980001
14 29961477 intron variant C/T snv 2.7E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs72662240
rs72662240
1.000 0.080 14 30093720 intron variant C/A snv 0.13
CUI: C0002170
Disease: Alopecia
Alopecia
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs8016859
rs8016859
14 30015516 intron variant G/C snv 3.2E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs1383618278
rs1383618278
1.000 0.080 14 29666158 missense variant G/A snv 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs1057519635
rs1057519635
1.000 14 29626508 missense variant C/T snv
CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA
0.800 0