Disease: Diastolic blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs1250259
FN1 ; LOC105373868
1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 5
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5
rs3741378
SIPA1
0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 3
rs936226 15 74776941 intergenic variant C/T snv 0.69 3