Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs567058829
TNN
1 175142624 intron variant -/A ins 1
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs112925537
INO80
15 41042015 intron variant -/C ins 2
rs10628234 15 74918801 downstream gene variant -/CA delins 2
rs146669915
SOX6
11 16269264 intron variant -/CTGT delins 1
rs138475089 7 100899019 upstream gene variant -/TA delins 1
rs35123175
HSF2BP
21 43586730 intron variant A/- delins 6.0E-02 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
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
rs13405173
PDE1A
2 182449087 intron variant A/C snv 8.8E-03 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
rs12741980 1 11879536 non coding transcript exon variant A/C snv 5.8E-02 2
rs12829468
LINC02398
12 20043911 intron variant A/C snv 0.61 2
rs12958173
LINC01478
18 44562012 intron variant A/C snv 0.70 2
rs16853958
LOC105371692
1 204559216 downstream gene variant A/C snv 0.59 2
rs28663144
SVEP1
9 110436611 intron variant A/C snv 4.9E-02 2
rs459588
ZNF831
20 59139712 intron variant A/C snv 0.21 2
rs6565174
LOC101928595
16 30100583 intron variant A/C snv 0.93 2
rs7297416
HOXC4
12 54049306 intron variant A/C snv 0.34 2
rs76326501
LOC105374567 ; LOC112268413
2 42940738 intergenic variant A/C snv 5.7E-02 2
rs7665304
LEF1
4 108104223 intron variant A/C snv 0.53 2
rs8105753 19 31436641 regulatory region variant A/C snv 0.33 2