CSMD1, CUB and Sushi multiple domains 1, 64478

N. diseases: 18; N. variants: 64
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: rs12541020
rs12541020 		1.000 0.040 8 4960070 intron variant T/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs1658820
rs1658820 		8 4431055 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs10046758
rs10046758 		1.000 0.040 8 4326648 non coding transcript exon variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs11787412
rs11787412 		0.925 0.040 8 3276717 intron variant C/A;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs11787412
rs11787412 		0.925 0.040 8 3276717 intron variant C/A;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs13250365
rs13250365 		1.000 0.040 8 3155942 intron variant G/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1379326
rs1379326 		8 4760288 intron variant T/C;G snv
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		Respiratory Tract Diseases 0.800 1.000 1 2013 2013
dbSNP: rs139425113
rs139425113 		1.000 0.040 8 4323090 intron variant A/-;AA;AAA delins
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs147739031
rs147739031 		1.000 0.080 8 3389886 intron variant A/C;G snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2014 2014
dbSNP: rs17070309
rs17070309 		8 4442361 intron variant G/A;T snv
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17079516
rs17079516 		1.000 0.040 8 3166618 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17404163
rs17404163 		8 4093523 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2046197
rs2046197 		1.000 0.080 8 3762230 intron variant G/A;C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs2449215
rs2449215 		8 3630816 intron variant A/C;G;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs2688326
rs2688326 		8 3910101 intron variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs270077
rs270077 		8 3422704 splice region variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs270091
rs270091 		8 3416389 intron variant C/A;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2938236
rs2938236 		8 3430160 intron variant A/C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4395908
rs4395908 		1.000 0.120 8 4168122 intron variant C/A;G snv
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs4633074
rs4633074 		8 4924352 intron variant G/A;C;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4875102
rs4875102 		1.000 0.040 8 4427170 intron variant G/A;T snv
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration 		Musculoskeletal Diseases 0.800 1.000 1 2013 2013
dbSNP: rs596332
rs596332 		1.000 0.040 8 3013429 intron variant T/A;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs62480124
rs62480124 		8 3921114 intron variant G/A;C;T snv
CUI: C4505222
Disease: Sleep Onset Latency
Sleep Onset Latency 		0.700 1.000 1 2016 2016
dbSNP: rs6558872
rs6558872 		0.882 0.040 8 4380617 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs6558872
rs6558872 		0.882 0.040 8 4380617 intron variant G/A;C snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2013 2013