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
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 5
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 5
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 5
rs1030431 8 58399138 intergenic variant A/G;T snv 3
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 3
rs17725246
NPC1L1
7 44542387 upstream gene variant T/A;C snv 3
rs1883711 20 40551182 regulatory region variant G/C snv 2.5E-02 3
rs34042070
TXNL4B ; HPR
16 72067626 intron variant C/G snv 0.17 3