Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs10046
MIR4713HG ; CYP19A1
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 6
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10203853
MROH2A
1.000 0.080 2 233778772 intron variant A/G;T snv 3
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs10211
CYP3A7 ; CYP3A7-CYP3A51P ; ZSCAN25
1.000 0.080 7 99705371 3 prime UTR variant T/C snv 0.25 1
rs1021737
CTH
0.925 0.120 1 70439117 missense variant G/T snv 0.28 0.24 2
rs1031245702
COL11A2
1.000 0.080 6 33171534 missense variant A/G snv 4.0E-06 1
rs10318
GREM1
0.882 0.080 15 32733778 3 prime UTR variant C/T snv 0.16 3
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 1
rs10380
MTRR
0.807 0.200 5 7897078 missense variant C/T snv 0.16 0.18 6
rs1040264140
FURIN
1.000 0.080 15 90881744 missense variant A/G snv 2
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 5
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 23
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042821
MSH6
0.732 0.280 2 47783349 missense variant G/A;C;T snv 0.18; 8.6E-06 16
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs1044471
ADIPOR2
1.000 0.080 12 1787790 3 prime UTR variant C/T snv 0.38 4
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34