Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801020
GRK6 ; F12 ; SLC34A1
1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 4
rs12133576
DR1
1.000 0.040 1 93350843 intron variant A/G snv 0.51 3
rs17036328
PPARG
1.000 0.040 3 12348985 intron variant T/C snv 0.14 3
rs17056278
EBF1
0.925 0.040 5 158825430 intron variant C/G snv 5.3E-02 3
rs478093
PHGDH ; LOC105378937
1.000 0.040 1 119712503 5 prime UTR variant A/G snv 0.73 3
rs4969186
PGS1
1.000 0.040 17 78402323 intron variant G/C snv 0.62 3
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs7544735
RNU6ATAC35P
1.000 0.040 1 220825571 intron variant G/A snv 0.22 3
rs8088980
ZNF407
1.000 0.040 18 74666435 intron variant C/T snv 0.51 3
rs8177248
TF
1.000 0.040 3 133760782 non coding transcript exon variant C/T snv 0.28 3
rs8177253
TF
1.000 0.040 3 133761348 non coding transcript exon variant C/T snv 0.31 3
rs10757022
SAXO1
1.000 0.040 9 19023615 intron variant A/G snv 0.51 2
rs10887868
PRXL2A
1.000 0.040 10 80434508 3 prime UTR variant G/A snv 0.34 2
rs11264339 1.000 0.040 1 155168172 downstream gene variant C/T snv 0.56 2
rs11639856
TNRC6A
1.000 0.040 16 24777324 missense variant T/A snv 0.17 0.19 2
rs1171114
PRSS35
1.000 0.040 6 83517927 intron variant T/C snv 0.59 2
rs12199222
NUP153
1.000 0.040 6 17699091 intron variant G/A;T snv 2
rs13395354
ACOXL
1.000 0.040 2 110842942 intron variant C/T snv 0.18 2
rs1635183
THSD7A
1.000 0.040 7 11643752 intron variant C/A;G snv 2
rs17093914
DLST
1.000 0.040 14 74896938 intron variant C/G;T snv 2
rs17109512
LOC105378449
1.000 0.040 10 98367794 regulatory region variant G/A snv 9.5E-02 2
rs17806888
SUCLG2
1.000 0.040 3 67365898 intron variant T/C snv 9.1E-02 2
rs2243834
RAB10
1.000 0.040 2 26134879 intron variant G/C;T snv 2
rs2452877 1.000 0.040 5 4027643 regulatory region variant A/G snv 0.60 2
rs2562456
LINC00664
1.000 0.040 19 21483408 non coding transcript exon variant C/T snv 0.77 2