Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs10949662
PTPRN2
7 157741413 intron variant C/A;T snv 2
rs10961430
NFIB
1.000 0.040 9 14224064 intron variant G/C;T snv 2
rs1108842
GNL3 ; PBRM1
3 52686064 5 prime UTR variant A/C;G;T snv 0.49; 4.0E-06 2
rs11130
NDE1 ; MYH11
1.000 0.040 16 15724453 3 prime UTR variant G/A;C snv 0.56; 4.0E-06 2
rs111342015
TTBK1
1.000 0.080 6 43259403 intron variant G/A;T snv 2
rs11166628
LINC02055
1.000 0.040 8 136066082 intron variant G/A;C snv 2
rs11588857
LRRN2 ; LOC105371692
1 204617919 missense variant G/A;T snv 0.20; 8.0E-06 2
rs11617058 1.000 0.040 13 84718977 intergenic variant T/C;G snv 2
rs11717383 1.000 0.040 3 52253452 downstream gene variant G/C;T snv 2
rs11793831 9 23362313 intron variant G/A;T snv 2
rs118134876
THSD7A
7 11460745 missense variant C/A;T snv 4.0E-02 2
rs12421382 1.000 0.040 11 109507345 intron variant C/G;T snv 2
rs12532143
IMMP2L
1.000 0.040 7 111385892 intron variant T/A;C snv 2
rs12914495
DENND4A
15 65687454 intron variant A/G;T snv 2
rs12967828 1.000 0.040 18 38549487 intergenic variant A/C;T snv 2
rs12991836
ZEB2
1.000 0.040 2 144383974 intron variant A/C;T snv 2
rs13136968
GPM6A
1.000 0.040 4 175713861 intron variant G/A;T snv 2
rs13220261
LOC107986583 ; BTN1A1
6 26498957 upstream gene variant C/A;T snv 2
rs1349265
THRB
1.000 0.040 3 24117896 3 prime UTR variant A/C;G snv 2
rs1363119 1.000 0.040 19 18333999 downstream gene variant A/G;T snv 2
rs144447022
LOC101929006
1.000 0.040 6 29276442 intron variant G/C;T snv 2
rs1456297 15 51672013 regulatory region variant C/A;G;T snv 2
rs1560208 1.000 0.040 5 89990437 intron variant C/A;G;T snv 2
rs16953305 1.000 0.040 16 54278937 downstream gene variant A/C;G snv 2