Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9272219
HLA-DQA1
0.925 0.160 6 32634492 intron variant G/T snv 0.29 4
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4
rs9467626
SLC17A3
0.882 0.160 6 25873518 intron variant C/A snv 7.3E-02 4
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 3
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 3
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs2070016
FGA
1.000 0.040 4 154589162 intron variant A/G snv 0.12 3
rs629444
H2BP5
0.882 0.160 6 25885586 non coding transcript exon variant C/T snv 0.17 3
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 3
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 3
rs253
LPL
1.000 0.040 8 19953906 intron variant C/T snv 0.53 3
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 3
rs707939
MSH5-SAPCD1 ; MSH5
0.851 0.200 6 31758911 intron variant C/A snv 0.34 0.26 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 3
rs13199775
SLC17A1
0.882 0.160 6 25828554 intron variant A/T snv 7.4E-02 3