ZNF536, zinc finger protein 536, 9745

N. diseases: 6; N. variants: 16
Source: CURATED ×
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: rs746961
rs746961 		19 30608983 intron variant A/G snv 0.46
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 1.000 1 2007 2007
dbSNP: rs2053079
rs2053079 		1.000 0.040 19 30496516 intron variant A/G snv 0.19
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.710 1.000 6 2014 2019
dbSNP: rs33439
rs33439 		19 30454264 intron variant C/T snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs10518269
rs10518269 		19 30537759 intron variant C/T snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11084553
rs11084553 		19 30528873 intron variant A/G snv 9.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11666918
rs11666918 		19 30543767 intron variant G/A snv 0.10
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12459057
rs12459057 		0.925 0.040 19 30505618 intron variant A/G snv 0.11
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs12459057
rs12459057 		0.925 0.040 19 30505618 intron variant A/G snv 0.11
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs12972995
rs12972995 		19 30250716 intron variant G/C snv 0.27
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs16964543
rs16964543 		1.000 0.080 19 30694303 intron variant T/C snv 0.32
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs16964543
rs16964543 		1.000 0.080 19 30694303 intron variant T/C snv 0.32
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs33428
rs33428 		19 30446936 intron variant A/G snv 0.71
CUI: C0026848
Disease: Myopathy
Myopathy 		Musculoskeletal Diseases; Nervous System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs33431
rs33431 		1.000 0.040 19 30449082 intron variant C/T snv 0.55
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs3786800
rs3786800 		1.000 0.040 19 30499793 intron variant T/C snv 0.17
CUI: C0154778
Disease: Myopia, Degenerative
Myopia, Degenerative 		Eye Diseases 0.700 1.000 1 2012 2012
dbSNP: rs4805531
rs4805531 		19 30245471 intron variant A/G snv 0.27
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs4805566
rs4805566 		19 30427409 intron variant T/A snv 0.67
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs7254263
rs7254263 		19 30250350 intron variant C/T snv 0.29
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs8109875
rs8109875 		1.000 0.040 19 30578732 intron variant G/A snv 0.11
CUI: C0024530
Disease: Malaria
Malaria 		Infections 0.700 1.000 1 2018 2018