Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10503253
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.850 0.889 1 2011 2017
dbSNP: rs10503256
rs10503256
CSMD1
1.000 0.040 8 4356657 intron variant A/G snv 0.57
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 2 2011 2012
dbSNP: rs10503253
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs1379326
rs1379326
CSMD1
8 4760288 intron variant T/C;G snv
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		0.800 1.000 1 2013 2013
dbSNP: rs4875102
rs4875102
CSMD1
1.000 0.040 8 4427170 intron variant G/A;T snv
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration 		0.800 1.000 1 2013 2013
dbSNP: rs73660619
rs73660619
CSMD1
1.000 0.080 8 3230651 intron variant T/C snv 6.8E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 1.000 1 2014 2014
dbSNP: rs10088247
rs10088247
CSMD1
1.000 0.040 8 3826677 intron variant C/T snv 0.76
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2010 2010
dbSNP: rs11136613
rs11136613
CSMD1
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: rs147739031
rs147739031
CSMD1
1.000 0.080 8 3389886 intron variant A/C;G snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.700 1.000 1 2014 2014
dbSNP: rs166582
rs166582
CSMD1 ; LOC105377791
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: rs17066135
rs17066135
CSMD1
8 3435346 intron variant G/A snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17067182
rs17067182
CSMD1
1.000 0.040 8 3729296 intron variant G/A snv 0.20
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2011 2011
dbSNP: rs17070309
rs17070309
CSMD1
8 4442361 intron variant G/A;T snv
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2449215
rs2449215
CSMD1
8 3630816 intron variant A/C;G;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs270067
rs270067
CSMD1 ; LOC105377791
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: rs270073
rs270073
CSMD1 ; LOC105377791
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: rs270076
rs270076
CSMD1 ; LOC105377791
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: rs270077
rs270077
CSMD1 ; LOC105377791
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
CSMD1 ; LOC105377791
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: rs2922086
rs2922086
CSMD1 ; LOC105377791
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: rs2938236
rs2938236
CSMD1
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: rs7007032
rs7007032
CSMD1
1.000 0.040 8 3821924 intron variant C/T snv 0.75
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2010 2010