Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10009409
LOC105377273 ; LOC107986286
1.000 0.080 4 72989536 intergenic variant C/T snv 0.35 1
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1004030
MMP14
1.000 0.080 14 22836440 upstream gene variant T/C snv 0.39 1
rs1004072779
ERG
0.925 0.080 21 38403547 missense variant T/C snv 2.1E-05 2
rs10046
MIR4713HG ; CYP19A1
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10086908
PCAT1 ; LOC105375751
1.000 0.080 8 126999692 intron variant T/C snv 0.28 1
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 22
rs10122495
UBAP2
1.000 0.080 9 34049781 upstream gene variant T/A snv 0.73 1
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs1016342
PCAT1 ; CASC19 ; PRNCR1 ; PCAT2
1.000 0.080 8 127080210 non coding transcript exon variant C/G;T snv 1
rs1016343
PCAT2 ; PCAT1 ; PRNCR1 ; CASC19
0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 8
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10175368
CYP1B1 ; CYP1B1-AS1
0.925 0.080 2 38080719 intron variant C/T snv 0.23 4
rs10187424
VAMP8
0.925 0.080 2 85567174 intron variant T/A;C snv 2
rs10194115
TTC7A
0.925 0.120 2 47012873 intron variant G/T snv 0.10 2
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1031588
PCAT2 ; PRNCR1 ; PCAT1 ; CASC19
1.000 0.080 8 127081032 non coding transcript exon variant C/A snv 0.24 1
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30 5
rs1034866440
AR
0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 4
rs1041258260
XRCC1
0.925 0.080 19 43552170 missense variant C/T snv 8.0E-06 1.4E-05 2
rs1041449 1.000 0.080 21 41529494 intron variant A/G snv 0.42 1