Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 4
rs7671167
FAM13A
0.925 0.040 4 88962828 intron variant C/T snv 0.53 4
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 4
rs13180
IREB2
0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 4
rs12373142
SPPL2C ; MAPT-AS1
0.851 0.200 17 45846834 missense variant C/G;T snv 0.15 4
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs13118928 0.925 0.040 4 144565237 intron variant A/G snv 0.33 3
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 3
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 3
rs7068966
CDC123
1.000 0.040 10 12235993 intron variant C/T snv 0.43 3
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 3
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 3
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 3
rs1903003
FAM13A
0.925 0.080 4 88965146 intron variant C/G;T snv 3
rs2763979
HSPA1B
0.827 0.360 6 31826815 upstream gene variant C/T snv 0.45 3
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 3