Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12
rs2507800
ANGPT1
1.000 0.040 8 107250441 3 prime UTR variant T/A snv 0.36 2
rs3756261
EGF
0.925 0.160 4 109911150 upstream gene variant T/C snv 9.9E-02 2
rs7576192 1.000 0.040 2 120360455 intergenic variant A/G snv 0.68 2
rs7579169 1.000 0.040 2 120360548 intergenic variant T/C snv 0.68 2
rs2198532
DCDC2C
1.000 0.040 2 3827777 intron variant T/C snv 0.79 1
rs770016471
ACE
1.000 0.040 17 63497260 missense variant C/G snv 1.4E-05 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1177506410
AGT
0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06 12
rs2059806
INSR
0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7
rs780972489
ISYNA1
1.000 0.040 19 18436831 synonymous variant C/T snv 8.9E-06 7.0E-06 1
rs779370907
ISYNA1
1.000 0.040 19 18436405 synonymous variant C/T snv 6.0E-05 1.4E-05 1
rs11549467
HIF1A ; HIF1A-AS3
0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1800595
F5
0.925 0.080 1 169541110 missense variant T/C;G snv 5.7E-02 2