Disease: Systolic Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs7832708
MSRA
8 10332530 intron variant C/T snv 0.49 4
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs6731373
LOC107985892
2 68275912 intergenic variant G/A snv 0.29 3
rs7963801
SYT1
12 79291446 intron variant T/C snv 0.70 3
rs17245822 13 72557556 intergenic variant A/C snv 0.34 2
rs258951 5 92718160 intergenic variant T/A snv 0.55 2