Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10961206 1.000 0.040 9 13724052 intron variant A/T snv 0.12 1
rs10981012
SHOC1
1.000 0.040 9 111690726 intron variant G/A snv 0.11 1
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 4
rs11022738 1.000 0.040 11 13271635 regulatory region variant T/C snv 0.32 1
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 3
rs11042937 1.000 0.040 11 10723847 upstream gene variant G/T snv 0.59 1
rs11057401
CCDC92
0.925 0.040 12 123942759 missense variant T/A snv 0.27 0.30 1
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 4
rs11057840
SCARB1
1.000 0.040 12 124831509 intron variant A/C snv 0.16 1
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs11072811
MORF4L1
1.000 0.040 15 78839988 intron variant A/C snv 0.51 1
rs11080107
ANKRD13B
1.000 0.040 17 29611406 intron variant T/A;C snv 1
rs11099493
RASGEF1B
1.000 0.040 4 81665896 intron variant A/C;G snv 1
rs11107903
LOC112268099 ; FGD6
1.000 0.040 12 95114195 intron variant G/A;C snv 1
rs111245230
SVEP1
1.000 0.040 9 110407495 missense variant T/C snv 2.6E-02 2.3E-02 3
rs111684993 1.000 0.040 15 41144539 intergenic variant A/G snv 0.32 1
rs11170820
FLJ12825
1.000 0.040 12 54120131 non coding transcript exon variant C/A;G snv 1
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 6
rs11191416
LOC107984264
1.000 0.040 10 102845159 intron variant T/G snv 0.10 1
rs112009435 1.000 0.040 19 17736035 upstream gene variant G/A;C snv 1
rs11204085
LOC105379311
1.000 0.040 8 20083285 intron variant T/C snv 0.38 1
rs11204666
ADAMTSL4-AS1
1.000 0.040 1 150570652 intron variant C/G;T snv 1
rs11204892 1.000 0.040 1 151795572 upstream gene variant A/G;T snv 1
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4