Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs10035650
KIAA0825
5 94600780 intron variant A/G snv 0.37 1
rs1005464
BMP2
0.882 0.040 20 6775501 intron variant G/A snv 0.19 5
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10074991
PRKAA1
0.851 0.120 5 40790449 intron variant G/A snv 0.31 7
rs10109984
PRKDC
0.925 0.080 8 47891114 intron variant T/C snv 0.54 4
rs1012049
PTPRK
6 128209162 intron variant G/A snv 0.44 2
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs10131
LIG4
1.000 0.040 13 108207498 3 prime UTR variant C/T snv 0.12 3
rs10132552
MEG3
1.000 0.040 14 100834675 non coding transcript exon variant T/C snv 0.25 3
rs10138053 14 51148434 intergenic variant T/C snv 0.74 1
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 6
rs10160246
LOC105376591
11 23153770 upstream gene variant A/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
rs1018379423
EPHB2
1 22907986 missense variant G/T snv 4.0E-06 2.1E-05 4
rs1019340046
TP53
0.882 0.080 17 7674225 missense variant C/T snv 5
rs10203853
MROH2A
1.000 0.080 2 233778772 intron variant A/G;T snv 5
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10248565
HDAC9
1.000 0.040 7 18935100 intron variant T/G snv 0.14 3
rs10272859
CDK14
0.925 0.120 7 90689160 intron variant G/C snv 0.39 4
rs10273639
PRSS1
0.776 0.280 7 142749077 upstream gene variant T/A;C snv 9