Disease: Blood Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10143078
COX16 ; SYNJ2BP-COX16 ; SYNJ2BP
14 70414772 intron variant A/C snv 6.6E-02 2
rs12195230
KLHL32
6 97052171 intron variant G/C snv 0.23 2
rs1421811
NPR3
5 32714164 intron variant C/G;T snv 2
rs2196122
MMP26
11 4864318 intron variant G/C snv 0.14 2
rs3096277
CDH13 ; LOC105371366
16 83730599 intron variant T/C snv 0.74 2
rs6782531
FHIT
3 61009928 intron variant G/C;T snv 2
rs7213273
NMT1
17 45078546 intron variant G/A snv 0.73 2
rs11105354
ATP2B1
12 89632746 intron variant A/G snv 0.15 3
rs11222084
ZBTB44-DT
11 130403335 non coding transcript exon variant A/T snv 0.30 3
rs1156725
SOX6
11 16286154 intron variant C/T snv 0.78 3
rs13002573 2 164058698 intron variant A/G snv 0.20 3
rs1401454
SOX6
11 16228637 intron variant C/A;G;T snv 3
rs17080102
PLEKHG1
6 150683634 5 prime UTR variant G/C snv 8.6E-02 3
rs17428471 7 27298248 intergenic variant G/T snv 9.4E-02 3
rs2014408
SOX6
11 16343736 intron variant C/T snv 0.17 3
rs2969070 7 2472910 downstream gene variant G/A;C snv 3
rs4842666 12 89547772 non coding transcript exon variant T/C snv 0.16 3
rs6026748
ZNF831
20 59170760 intron variant G/A snv 0.14 3
rs6825911
ENPEP
4 110460482 intron variant C/T snv 0.68 3
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 4
rs1446468 2 164106976 intron variant T/C snv 0.40 4
rs17477177 1.000 0.080 7 106771412 upstream gene variant T/C snv 0.17 4
rs2493134
AGT
1 230713613 intron variant T/C snv 0.57 4
rs2782980
LOC105378492
10 114021768 regulatory region variant T/C snv 0.66 4
rs319690
MAP4
3 47885994 intron variant T/C snv 0.39 4