Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10155855 7 111688341 intergenic variant A/T snv 0.12 1
rs10156191
LOC105375567 ; AOC1
7 150856517 missense variant C/T snv 0.26 0.33 1
rs10156578 9 29372503 intergenic variant C/A;G;T snv 1
rs10166942
TRPM8
0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40 4
rs10218452
LOC105378606 ; PRDM16
1 3159033 intron variant A/G snv 0.23 1
rs1024905 1.000 0.040 12 4408974 downstream gene variant G/A;C snv 2
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
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs1043994
NOTCH3
0.827 0.120 19 15192033 synonymous variant T/A;C snv 4.0E-06; 0.85 7
rs10456100
KCNK5
1.000 0.040 6 39215694 intron variant C/T snv 0.20 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1047964
BACE1 ; RNF214
11 117286177 3 prime UTR variant G/A;C;T snv 3
rs104894561
CSNK1D
0.882 0.120 17 82265743 missense variant T/C snv 4.0E-06 7.0E-06 5
rs1049793
LOC105375567 ; AOC1
0.882 0.080 7 150860577 missense variant C/G;T snv 0.37 0.37 4
rs1050316
MEF2D
1 156464911 3 prime UTR variant G/T snv 0.54 3
rs10504861
LOC105375630 ; LOC105375629
0.925 0.040 8 88535703 intron variant C/T snv 0.23 3
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10737909 1 15222140 upstream gene variant G/T snv 0.45 1
rs10786156
PLCE1
10 94254865 intron variant C/G snv 0.44 0.47 2
rs10803531
GPR39
2 132469969 intron variant A/C;T snv 1
rs10849061 12 4414290 intergenic variant C/T snv 0.43 1
rs10871745 18 57511578 intergenic variant A/G snv 0.71 1