Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36067435
ELOVL6
1.000 0.040 4 110180390 intron variant -/TTAT delins 1
rs1902023
UGT2B15
0.882 0.080 4 68670366 missense variant A/C snv 0.51 0.53 4
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 7
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs17144046 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 4
rs16902947 1.000 0.040 5 36308995 intergenic variant A/G snv 0.22 1
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs141179786 1.000 0.040 18 53662174 intergenic variant A/G;T snv 2.2E-02 1
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs200476 1.000 0.040 6 27800570 intergenic variant A/T snv 0.28 2
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs1045531
PSCA
0.882 0.080 8 142682129 synonymous variant C/A snv 0.45 0.44 3
rs72551387
UGT2B17
0.882 0.080 4 68568232 missense variant C/A snv 5.7E-03 5.7E-03 3
rs680055
CYP3A43
0.851 0.120 7 99859982 missense variant C/A;G snv 6.5E-02 0.13 5
rs10459953
NOS2
0.925 0.080 17 27800492 5 prime UTR variant C/A;G;T snv 3
rs2364480
LTBR
0.925 0.120 12 6386109 synonymous variant C/A;T snv 0.77; 2.0E-05 2
rs6078585 1.000 0.040 20 12447612 intergenic variant C/A;T snv 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs6561599
DLEU1 ; RNASEH2B-AS1
1.000 0.040 13 50904782 non coding transcript exon variant C/G snv 0.61 2