Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs1037733674
GCG ; LOC101929532
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10489177
C1orf112 ; METTL18
0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 4
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1057293
SGK1
0.925 0.120 6 134172259 synonymous variant G/A snv 0.12 0.11 4
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11124945
PLEKHH2
1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs113296370
PLEKHH2
1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11712619
KALRN
0.882 0.160 3 124300955 intron variant C/A;T snv 0.26 5
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11