Disease: Cardiovascular Diseases
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 8
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 6
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs1275988
KCNK3
1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5