Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3087969
SLC44A2
1.000 0.040 19 10627963 missense variant C/G;T snv 4.0E-06; 0.79 1
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs3840634
CAV1
0.925 0.120 7 116556798 intron variant T/C snv 2
rs2682826
NOS1
0.807 0.280 12 117215033 3 prime UTR variant G/A snv 0.25 11
rs41279104
NOS1
0.827 0.160 12 117439680 intron variant C/T snv 0.11 6
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1274867386
HMX2
1.000 0.040 10 123150118 missense variant T/A snv 7.0E-06 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
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
rs1052571
CASP9
0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 4
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs77485247
HRH4
0.925 0.080 18 24460578 upstream gene variant T/A snv 3
rs2075575
AQP4-AS1 ; AQP4
0.851 0.200 18 26866562 intron variant G/A snv 0.31 5
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
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1805127
KCNE1
0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17