Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs149379258 6 118333210 intergenic variant -/A delins 0.10 1
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs528266117
GLT8D1
3 52695764 non coding transcript exon variant -/ATTA delins 1.5E-03 1
rs112925537
INO80
15 41042015 intron variant -/C ins 2
rs35295665
CASZ1
1 10737371 intron variant -/C delins 2
rs10628234 15 74918801 downstream gene variant -/CA delins 2
rs35571646 11 100662632 upstream gene variant -/CTAT ins 0.34 1
rs34862067
ESR1
6 152018839 intron variant -/GAA delins 0.22 1
rs142065594 11 107220703 intergenic variant -/GT delins 0.40 1
rs111524356
CEP68 ; LOC107984063
2 65057022 intron variant -/GTGGATGCAGCAG;TGGATGCAGCAG;TGGATGCGGCAG;TGTATGCAGCAG delins 0.45 2
rs558074929
PPL
16 4889421 intron variant -/T;TT delins 1
rs368910700
EBF1
5 158894394 intron variant -/TAAA ins 0.32 1
rs142457531 2 190644147 intron variant -/TGAA delins 1
rs10712836 8 125498975 intron variant A/- delins 0.48 1
rs34271465
COBLL1
2 164656556 intron variant A/- delins 0.48 1
rs527953512
NRG1
8 32533038 intron variant A/-;AA;AAA;AAAA;AAAAAA delins 1
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 6
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs8098380
YES1
18 721563 downstream gene variant A/C snv 0.33 4
rs11731886
LOC105377506
4 155738667 downstream gene variant A/C snv 0.21 3
rs12032672
PKN2-AS1
0.925 0.040 1 88159953 intron variant A/C snv 0.37 3
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 3
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 3