Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs10022537
PROM1
0.925 0.080 4 16075214 intron variant A/T snv 0.70 2
rs1002765
CHMP2B ; MIR4795
0.851 0.080 3 87227912 intron variant G/A;C snv 4
rs10029005
LINC02516
1.000 0.080 4 124530209 intron variant G/A snv 0.40 1
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs10052016
SLC6A3
0.925 0.080 5 1427996 intron variant A/G snv 0.22 2
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 7
rs10074991
PRKAA1
0.851 0.120 5 40790449 intron variant G/A snv 0.31 7
rs10088390
SFRP1
0.925 0.080 8 41264249 3 prime UTR variant C/G snv 0.19 2
rs1011445550
TP53
0.925 0.080 17 7676391 missense variant G/C snv 2
rs10116253 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 4
rs1016343
PCAT2 ; PCAT1 ; PRNCR1 ; CASC19
0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 8
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs10421916
INSL3
0.925 0.080 19 17818178 intron variant A/G snv 0.69 2
rs1042229
FPR1
0.790 0.280 19 51746419 missense variant A/C;G snv 0.32; 0.13 7
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1044432
BTBD10
0.925 0.080 11 13388251 3 prime UTR variant A/T snv 0.16 2
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10464867
OSGIN2 ; NBN
0.925 0.080 8 89933370 3 prime UTR variant C/T snv 3.0E-02 2
rs10474606
THBS4
0.925 0.080 5 80057163 intron variant G/A snv 0.28 2
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1047840
EXO1
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19