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: rs17115100
rs17115100
1.000 0.040 10 102831636 3 prime UTR variant G/T snv 0.14 0.10
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2009 2009
dbSNP: rs284844
rs284844
10 102794772 intron variant A/G snv 0.82
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 2 2017 2018
dbSNP: rs284844
rs284844
10 102794772 intron variant A/G snv 0.82
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2017 2018
dbSNP: rs6892
rs6892
10 102816113 3 prime UTR variant A/G snv 0.15
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 2 2019 2019
dbSNP: rs11191392
rs11191392
1.000 0.040 10 102767194 intron variant C/A snv 0.49
CUI: C0003467
Disease: Anxiety
Anxiety
0.700 1.000 1 2018 2018
dbSNP: rs139247810
rs139247810
10 102801321 intron variant T/G snv 3.0E-03
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs284844
rs284844
10 102794772 intron variant A/G snv 0.82
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs284859
rs284859
10 102813260 missense variant G/A;T snv 8.1E-06; 0.20
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs284860
rs284860
10 102813206 missense variant T/C snv 0.59 0.57
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs3740397
rs3740397
1.000 0.040 10 102832918 3 prime UTR variant G/C snv 0.35
CUI: C0003467
Disease: Anxiety
Anxiety
0.700 1.000 1 2018 2018
dbSNP: rs4919683
rs4919683
10 102825368 intron variant C/A;T snv
CUI: C0337443
Disease: Sodium measurement
Sodium measurement
0.700 1.000 1 2018 2018
dbSNP: rs562752749
rs562752749
10 102805443 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTT;TTTTTTTTTTTT delins
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs562752749
rs562752749
10 102805443 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTT;TTTTTTTTTTTT delins
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs73351820
rs73351820
10 102810527 intron variant T/A;C;G snv
CUI: C0201952
Disease: Chloride measurement
Chloride measurement
0.700 1.000 1 2018 2018