Disease: Mean blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6461992
HOXA10-HOXA9 ; HOXA11 ; HOXA10
1.000 0.120 7 27181212 3 prime UTR variant A/G snv 0.93 4
rs4722675
HOTTIP
7 27204343 intron variant A/G snv 0.93 4
rs3735533
HOTTIP
7 27206274 non coding transcript exon variant T/C snv 0.93 4
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs2999159
MOV10
1 112688136 intron variant A/G snv 0.85 4
rs2881854
ENPEP
4 110422107 intron variant C/A snv 0.83 2
rs284844
WBP1L
10 102794772 intron variant A/G snv 0.82 3
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs2286525
TBX2-AS1
17 61394762 intron variant G/A snv 0.73 3
rs7302981
CERS5
12 50144032 missense variant A/G;T snv 0.69 0.71 4
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71 5
rs1407040
GNAS
20 58897119 intron variant C/T snv 0.70 4
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs12630213
FGD5
3 14912904 intron variant C/T snv 0.68 4
rs2240736
TBX2
17 61408032 non coding transcript exon variant C/T snv 0.64 0.68 4
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs2782980
LOC105378492
10 114021768 regulatory region variant T/C snv 0.66 3
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 5
rs4551304
PINX1
8 10807559 intron variant A/G snv 0.65 3
rs900145 11 13272358 upstream gene variant C/T snv 0.62 4
rs7928655
ARNTL
11 13278705 intron variant C/G snv 0.61 2
rs4910498
SWAP70
11 9743956 intron variant A/T snv 0.61 4