Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10137527 14 105134327 intron variant C/T snv 8.3E-02 1
rs10226458 7 47595969 intergenic variant T/A snv 0.65 1
rs10423902 19 33273956 intergenic variant G/A;T snv 1
rs1075871 3 194960568 regulatory region variant G/A snv 0.36 1
rs10774599 12 110259643 intergenic variant T/G snv 0.43 1
rs10779596 1 212903562 downstream gene variant G/T snv 0.61 1
rs1088639 16 41062 upstream gene variant G/C snv 1.4E-02 1
rs10973267 9 3734162 intergenic variant G/A snv 0.45 1
rs11122219 1 231067843 intergenic variant C/T snv 0.18 1
rs111271889 19 14070187 upstream gene variant A/G snv 0.48 1
rs11136012 8 27842198 upstream gene variant A/C snv 0.61 1
rs111437842 13 40691846 intergenic variant T/A;C snv 4.9E-02 1
rs11171731 12 56049558 downstream gene variant C/T snv 0.34 1
rs111821611 19 12443819 intron variant G/A snv 0.43 1
rs11199878 10 121282307 intergenic variant A/T snv 0.19 1
rs11428167 3 196184704 intergenic variant -/T delins 0.13 1
rs11583750 1 47564678 regulatory region variant G/A snv 6.6E-02 1
rs11615482 12 4222038 intergenic variant C/A snv 0.22 1
rs11657639 17 48470102 downstream gene variant A/G snv 0.43 1
rs11674773 2 189502331 intergenic variant A/G snv 0.23 1
rs11708187 3 72347178 intergenic variant G/A snv 0.26 1
rs117288711 8 103390144 intergenic variant C/A snv 5.2E-02 1
rs117473347 16 88990805 intron variant G/A snv 3.1E-02 1
rs11777872 8 63612789 upstream gene variant A/G snv 0.87 1
rs117849885 11 103020694 intergenic variant A/C snv 1.5E-02 1