Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10175338
CYP1B1-AS1 ; CYP1B1
0.925 0.080 2 38080501 intron variant G/T snv 0.25 2
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs1020475809
NQO1
0.925 0.080 16 69711027 synonymous variant A/G snv 2.0E-05 7.0E-06 2
rs10216653
CHRAC1
0.882 0.080 8 140516886 3 prime UTR variant G/C snv 0.80 3
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10269006 1.000 0.080 7 94758031 intergenic variant G/T snv 0.32 1
rs10273424
TMEM225B
0.925 0.080 7 99598450 intron variant T/A snv 0.13 3
rs1028842
RAD51B
1.000 0.080 14 68205006 intron variant C/A snv 0.17 1
rs1029342144
KLLN ; PTEN
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv 6
rs1029946
PRKAG2
0.925 0.080 7 151578720 intron variant A/G snv 0.21 2
rs1033662
LINC01524 ; LOC105372666
0.925 0.080 20 52408842 intron variant A/G snv 0.46 2
rs1034794 0.925 0.080 7 124801348 intergenic variant A/T snv 0.69 2
rs1036980234
PTCH1
0.827 0.160 9 95447156 missense variant G/A snv 6
rs10380
MTRR
0.807 0.200 5 7897078 missense variant C/T snv 0.16 0.18 6
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58 4
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1041983
NAT2
0.732 0.240 8 18400285 synonymous variant C/T snv 0.34 0.36 15
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042638
TPD52
0.925 0.080 8 80037711 3 prime UTR variant G/A;T 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