Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16896923
ZNRD1ASP ; ETF1P1
1.000 0.120 6 30032910 non coding transcript exon variant T/C snv 5.0E-02 1
rs2191566
ZNF230
0.925 0.200 19 44007237 intron variant G/T snv 0.62 2
rs9623117
TNRC6B
0.851 0.200 22 40056115 intron variant T/C snv 0.38 2
rs9510787
TNFRSF19
1.000 0.120 13 23631056 intron variant A/G snv 0.20 1
rs1465618
THADA
0.882 0.160 2 43326810 intron variant T/C snv 0.80 2
rs748404
TGM5
0.851 0.160 15 43267033 upstream gene variant T/C snv 0.17 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 1
rs8102476
SPINT2
0.776 0.240 19 38244973 intron variant C/T snv 0.40 2
rs13397985
SP110 ; SP140
0.827 0.280 2 230226508 intron variant T/C;G snv 3
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 2
rs9364554
SLC22A3
0.882 0.160 6 160412632 intron variant C/T snv 0.21 2
rs651164
SLC22A1
0.882 0.160 6 160160342 downstream gene variant A/G snv 0.69 2
rs2305806
SH2D3A
1.000 0.120 19 6754996 synonymous variant T/C snv 0.30 0.35 1
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 4
rs4809324
RTEL1 ; RTEL1-TNFRSF6B
0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02 3
rs2180341
RNF146
0.882 0.160 6 127279485 intron variant G/A snv 0.73 2
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 2
rs999737
RAD51B
0.776 0.200 14 68567965 intron variant C/T snv 0.16 2
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 4
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 3
rs11083846
PRKD2
0.882 0.200 19 46704397 splice region variant G/A snv 0.17 0.16 2
rs2284063
PLA2G6
0.851 0.160 22 38148291 non coding transcript exon variant A/G snv 0.40 3
rs910873
PIGU
0.882 0.160 20 34583968 intron variant G/A;C snv 2