Source: GWASCAT

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: rs4332037
rs4332037
1.000 0.040 7 1911173 intron variant C/T snv 0.19
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 1.000 1 2018 2018
dbSNP: rs527510716
rs527510716
1.000 0.080 7 1904901 intron variant G/C snv 0.14
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.700 1.000 1 2018 2018
dbSNP: rs56072378
rs56072378
1.000 0.040 7 2064729 intron variant A/G snv 0.29
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2018 2018
dbSNP: rs62442924
rs62442924
7 1950341 intron variant C/T snv 0.17
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs71525361
rs71525361
7 2120142 intron variant T/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs4721089
rs4721089
7 1833285 intron variant C/T snv 0.80
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs58120505
rs58120505
1.000 0.040 7 1990232 intron variant T/C snv 0.37
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 2 2019 2019
dbSNP: rs10950456
rs10950456
1.000 0.040 7 1940114 5 prime UTR variant G/A snv 0.57
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder
0.700 1.000 1 2019 2019
dbSNP: rs11763750
rs11763750
7 2040479 intron variant G/A snv 0.16
CUI: C0424574
Disease: Duration of sleep
Duration of sleep
0.700 1.000 1 2019 2019
dbSNP: rs11770148
rs11770148
7 1859811 intron variant A/G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs117829095
rs117829095
7 1892738 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs13234909
rs13234909
7 1827295 intron variant G/A snv 0.33
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs1860826
rs1860826
7 2072871 intron variant G/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2019 2019
dbSNP: rs34731055
rs34731055
7 2067293 intron variant C/T snv 0.13
CUI: C0424574
Disease: Duration of sleep
Duration of sleep
0.700 1.000 1 2019 2019
dbSNP: rs3800917
rs3800917
1.000 7 2128304 intron variant G/A snv 0.28
Adverse effects, not elsewhere classified
0.700 1.000 1 2019 2019
dbSNP: rs3823624
rs3823624
1.000 0.040 7 2070711 intron variant T/C snv 0.17
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2019 2019
dbSNP: rs3823624
rs3823624
1.000 0.040 7 2070711 intron variant T/C snv 0.17
CUI: C0424574
Disease: Duration of sleep
Duration of sleep
0.700 1.000 1 2019 2019
dbSNP: rs3996330
rs3996330
7 1979188 intron variant C/A snv 0.54
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs4721096
rs4721096
1.000 0.040 7 1837675 intron variant T/C snv 0.84
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
0.700 1.000 1 2019 2019
dbSNP: rs57633152
rs57633152
7 2002912 intron variant C/G snv 0.46
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs58120505
rs58120505
1.000 0.040 7 1990232 intron variant T/C snv 0.37
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2019 2019
dbSNP: rs6963853
rs6963853
7 1819089 intron variant G/A snv 0.48
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019