Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003346
TMEM245
1.000 9 109053060 intron variant C/A snv 0.43 2
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs10089084
IDO1
8 39912430 intron variant G/C snv 0.30 1
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10123021 9 100689786 regulatory region variant G/A;T snv 1
rs1035543
PKD1L3
16 71949873 missense variant G/C snv 0.39 0.33 2
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10414398
CEACAM20
19 44517149 missense variant G/A snv 0.14 0.15 1
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10432782
SOD1
0.807 0.160 21 31664078 intron variant T/G snv 0.19 7
rs10435816
IL33
1.000 0.080 9 6225535 intron variant A/G snv 0.35 2
rs1043994
NOTCH3
0.827 0.120 19 15192033 synonymous variant T/A;C snv 4.0E-06; 0.85 7
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10478723
EDN1
6 12295228 intron variant G/A snv 0.15 1
rs1048661
LOXL1-AS1 ; LOXL1
0.732 0.320 15 73927205 missense variant G/T snv 0.33 0.28 14
rs10488682
TPH1
1.000 0.160 11 18040935 5 prime UTR variant T/A snv 0.19 2
rs104894845
GLA ; RPL36A-HNRNPH2
0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04 8