Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4133289
LINC02819
1 159484147 downstream gene variant C/T snv 0.16 1
rs1160297
LOC105369165
2 53010182 intergenic variant G/C snv 0.69 1
rs4957325
LOC105374737 ; TTC33
5 40620480 intron variant C/G;T snv 1
rs11719450
LOC107986092
3 58471084 TF binding site variant C/T snv 0.28 1
rs530159671
LUC7L
16 200185 intron variant G/A snv 2.0E-03 1
rs544453779
MIDEAS
14 73751866 intron variant C/T snv 4.3E-03 1
rs66561647
MIR1205 ; PVT1
8 127959615 intron variant C/A;T snv 1
rs17006441
MITF
3 69792729 intron variant C/A snv 0.35 1
rs2230657
NASP
1 45607817 synonymous variant G/A snv 0.52 0.55 1
rs12548874
NDUFAF6
8 94922936 intron variant C/A snv 0.40 1
rs66782572
NT5DC2
3 52533601 missense variant A/G snv 0.48 0.51 1
rs184562466
PMS2P1
7 100325440 intron variant C/T snv 5.2E-03 1
rs1340818
POMP
13 28665493 intron variant T/C snv 0.48 1
rs4073770
PPARG
3 12326734 intron variant A/T snv 0.25 1
rs6665764
PROX1
1 214004080 intron variant G/A snv 0.27 1
rs7560180
PSD4
2 113207623 3 prime UTR variant A/C;T snv 1
rs116834467
PSORS1C3 ; POU5F1
6 31174193 intron variant C/A snv 1
rs557277320
RAB11A ; DENND4A
15 65757263 intron variant GGG/-;G;GG;GGGG;GGGGG;GGGGGG delins 1
rs447735
SPATA33
16 89667941 intron variant T/C snv 0.33 1
rs2246363
TEX41 ; LOC100505498
2 145025715 intron variant G/A snv 0.82 1
rs228918
TMPRSS6
22 37110640 upstream gene variant T/C snv 0.40 1
rs5756504
TMPRSS6
22 37071230 intron variant C/G;T snv 1
rs5756519
TMPRSS6
22 37112384 upstream gene variant G/C snv 0.41 1
rs5756520
TMPRSS6
22 37112467 upstream gene variant G/A snv 0.41 1
rs800911
TRPS1
8 115483682 intron variant T/A snv 0.26 1