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: rs10032729
rs10032729
4 14878321 intron variant G/A snv 0.61
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10043077
rs10043077
5 56397112 intergenic variant T/C snv 0.29
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs1004467
rs1004467
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 3 2009 2018
dbSNP: rs10048404
rs10048404
18 56911251 intron variant C/T snv 0.28
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2018 2019
dbSNP: rs10059921
rs10059921
5 88218698 intron variant G/T snv 5.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs10062049
rs10062049
5 62258054 regulatory region variant C/T snv 0.16
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2018 2019
dbSNP: rs10077885
rs10077885
5 115054424 regulatory region variant C/A snv 0.56
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2016 2018
dbSNP: rs1008058
rs1008058
5 123099932 missense variant G/A;T snv 0.17 0.12
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2016 2016
dbSNP: rs1009017
rs1009017
14 71999568 intron variant T/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10096777
rs10096777
8 10660990 intron variant G/A snv 0.61
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs10107145
rs10107145
8 10900703 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs1011018
rs1011018
7 139763465 intron variant G/A snv 0.30
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs1012089
rs1012089
16 74138074 intron variant C/G;T snv 0.40
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2018 2019
dbSNP: rs10143078
rs10143078
14 70414772 intron variant A/C snv 6.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2014 2014
dbSNP: rs10147464
rs10147464
14 98122398 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10149871
rs10149871
14 99645618 intron variant C/T snv 0.36
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs1014988
rs1014988
1 1748780 upstream gene variant G/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10158347
rs10158347
1 232393998 downstream gene variant A/G snv 0.31
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10160382
rs10160382
11 76416170 downstream gene variant T/C snv 0.39
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10166552
rs10166552
2 223171819 intron variant C/A;G;T snv 4.3E-03
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs10167839
rs10167839
2 181018152 intron variant G/A snv 0.39
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs1018148
rs1018148
15 48610929 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10182056
rs10182056
2 55463087 intergenic variant A/G snv 0.30
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10182307
rs10182307
2 227010644 intron variant G/A snv 0.48
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019