Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs426496
LOC101927318 ; AQP2
1.000 0.040 12 49954295 synonymous variant T/C snv 0.77 0.71 3
rs1274867386
HMX2
1.000 0.040 10 123150118 missense variant T/A snv 7.0E-06 1
rs17173510
KCNE1
1.000 0.040 21 34449551 synonymous variant C/G;T snv 4.0E-06; 3.6E-03 6.6E-03 1
rs2234688
IFNG-AS1 ; IFNG
1.000 0.040 12 68158742 intron variant -/G;TGAG;TGG;TGTGG;TGTGTGAG;TGTGTGG;TGTGTGTGG delins 1
rs3087969
SLC44A2
1.000 0.040 19 10627963 missense variant C/G;T snv 4.0E-06; 0.79 1
rs3746951
SIK1
1.000 0.040 21 43426136 missense variant C/A;T snv 0.23 1
rs487119
SLC8A1
1.000 0.040 2 40261737 intron variant G/A snv 0.54 1
rs1052571
CASP9
0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 4
rs77485247
HRH4
0.925 0.080 18 24460578 upstream gene variant T/A snv 3
rs3736309
LOC101927318 ; AQP5 ; LOC105369764
0.925 0.120 12 49964271 intron variant A/G snv 0.12 2
rs3840634
CAV1
0.925 0.120 7 116556798 intron variant T/C snv 2
rs28357984
ND2 ; COX1
0.851 0.160 MT 5178 missense variant C/A snv 6
rs41279104
NOS1
0.827 0.160 12 117439680 intron variant C/T snv 0.11 6
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs11096955
TLR10
0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41 5
rs2075575
AQP4-AS1 ; AQP4
0.851 0.200 18 26866562 intron variant G/A snv 0.31 5
rs1805127
KCNE1
0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs2682826
NOS1
0.807 0.280 12 117215033 3 prime UTR variant G/A snv 0.25 11
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 5
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62