Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2032487
MYH9
0.882 0.080 22 36299382 intron variant C/T snv 0.78 3
rs760336723
PODXL
0.882 0.240 7 131506292 missense variant G/A snv 2.8E-05 5.6E-05 3
rs538166970
ACE
0.925 0.080 17 63496920 missense variant G/A;C snv 1.6E-05; 4.0E-06 2
rs118203979
CLDN19
0.925 0.080 1 42740005 missense variant C/T snv 9.0E-05 2.8E-05 2
rs3024912
LOC105373805
0.925 0.120 2 191028361 intron variant A/C snv 0.29 2
rs437168
NPHS1
1.000 0.080 19 35843517 synonymous variant G/A;C snv 7.9E-02; 1.2E-05 2
rs367825197
PODXL
0.925 0.080 7 131509412 stop gained G/A snv 4.0E-06 2
rs2285450
KIRREL2 ; NPHS1
1.000 0.080 19 35851365 synonymous variant G/A snv 2.2E-02 4.1E-02 1
rs4821481
MYH9
1.000 0.080 22 36299896 intron variant C/T snv 0.78 1
rs200640958
TRPC6
1.000 0.080 11 101471303 synonymous variant G/A;C snv 8.0E-06; 1.6E-05 1
rs754919065
TRPC6
1.000 0.080 11 101504767 missense variant G/A snv 6.1E-05; 4.1E-06 7.0E-06 1