Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13204672 1.000 0.040 6 32615019 intergenic variant A/G snv 0.12 1
rs13208776
SMOC2
0.882 0.040 6 168540944 intron variant G/A;C snv 1
rs1417210
SLC29A3
0.925 0.040 10 71376162 intron variant G/A;C snv 1
rs1548514 1.000 0.040 6 30419691 downstream gene variant G/A;C;T snv 1
rs17008723
FOXP1
0.925 0.040 3 71523984 intron variant T/G snv 0.15 1
rs17188127
TRIM15
1.000 0.040 6 30167325 intron variant C/T snv 9.9E-03 1
rs17188268 1.000 0.040 6 30231581 downstream gene variant G/A snv 3.2E-02 1
rs17190134
HCG22
1.000 0.040 6 31054083 non coding transcript exon variant C/A;G snv 1
rs17195551
ATAT1
1.000 0.040 6 30633618 intron variant C/T snv 3.2E-02 1
rs2236313
RNASET2
1.000 0.040 6 166946901 intron variant T/C snv 0.53 0.50 1
rs2248902 1.000 0.040 6 31266337 downstream gene variant G/A;T snv 1
rs2456973
LOC105369781 ; IKZF4 ; LOC105369780
0.925 0.040 12 56023144 intron variant A/C;G snv 1
rs2523505
DDX39B ; ATP6V1G2-DDX39B ; DDX39B-AS1 ; SNORD84
1.000 0.040 6 31542225 5 prime UTR variant C/G snv 7.6E-02 1
rs28383344
LOC107986589 ; HLA-DQA1
1.000 0.040 6 32637290 intron variant C/G;T snv 1
rs2839511
UBASH3A
1.000 0.040 21 42428412 intron variant G/A;T snv 1
rs291700
CDK5RAP1
0.925 0.040 20 33394043 synonymous variant T/C snv 0.64 0.62 1
rs3130347
EGFL8 ; PPT2-EGFL8 ; PPT2
1.000 0.040 6 32166879 intron variant T/C snv 0.15 0.18 1
rs3130455
CCHCR1 ; TCF19
1.000 0.040 6 31158201 5 prime UTR variant A/C;T snv 1
rs3132649 1.000 0.040 6 30353280 downstream gene variant G/A snv 0.11 1
rs3213758
RPGRIP1L
0.925 0.040 16 53605526 missense variant C/T snv 7.3E-02 4.7E-02 1
rs3218822
VARS2 ; GTF2H4
1.000 0.040 6 30912559 intron variant T/C snv 1.9E-02 1
rs33986393 1.000 0.040 6 30456297 downstream gene variant A/G snv 0.16 1
rs34101875 1.000 0.040 6 30455581 non coding transcript exon variant G/A;C;T snv 1
rs35407515 1.000 0.040 6 30455446 non coding transcript exon variant A/G snv 0.17 1
rs35792611
LOC105375012
1.000 0.040 6 30463098 upstream gene variant C/G snv 0.16 1