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: rs270073
rs270073 		8 3424305 intron variant A/T snv 0.91
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs270067
rs270067 		8 3426042 intron variant A/C snv 0.90
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2922086
rs2922086 		8 3415331 intron variant A/G snv 0.89
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs166582
rs166582 		8 3423210 intron variant G/T snv 0.89
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs270076
rs270076 		8 3423046 intron variant G/T snv 0.89
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs673465
rs673465 		1.000 0.040 8 3000838 intron variant C/G snv 0.87
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2406305
rs2406305 		1.000 0.040 8 3160861 intron variant C/T snv 0.85
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10088247
rs10088247 		1.000 0.040 8 3826677 intron variant C/T snv 0.76
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs7007032
rs7007032 		1.000 0.040 8 3821924 intron variant C/T snv 0.75
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs2688325
rs2688325 		8 3909688 intron variant T/C snv 0.63
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs2627395
rs2627395 		8 3921330 intron variant C/T snv 0.58
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs10503256
rs10503256 		1.000 0.040 8 4356657 intron variant A/G snv 0.57
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.800 1.000 2 2011 2012
dbSNP: rs12550650
rs12550650 		8 4693468 intron variant C/T snv 0.49
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs7828501
rs7828501 		8 4702559 intron variant A/G snv 0.48
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs11136613
rs11136613 		8 3368683 intron variant T/A snv 0.44
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs17079504
rs17079504 		1.000 0.040 8 3161800 intron variant G/A snv 0.30
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4266671
rs4266671 		8 4971671 intron variant A/G snv 0.27
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs67121641
rs67121641 		8 4936142 intron variant C/G snv 0.26
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7463166
rs7463166 		8 4976268 intron variant A/G snv 0.26
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs13261217
rs13261217 		1.000 0.040 8 4325535 non coding transcript exon variant A/G snv 0.26
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs13260434
rs13260434 		0.925 0.040 8 3368702 intron variant T/A snv 0.24
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs13260434
rs13260434 		0.925 0.040 8 3368702 intron variant T/A snv 0.24
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11998250
rs11998250 		1.000 0.040 8 3162070 intron variant A/C snv 0.22
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs592700
rs592700 		1.000 0.040 8 3008823 intron variant T/C snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17067182
rs17067182 		1.000 0.040 8 3729296 intron variant G/A snv 0.20
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2011 2011