Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs1513272
JAZF1
7 28160478 intron variant C/T snv 0.40 4
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs2294239
ZNRF3
22 29053489 intron variant A/G snv 0.36 4
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs55747707
MLXIPL
7 73623036 intron variant G/A snv 0.16 4
rs6545714 2 59080590 intron variant G/A;C snv 4
rs6780171
IGF2BP2
3 185785668 intron variant T/A snv 0.39 4
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 4
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4
rs8066985 17 70457204 intergenic variant A/G snv 0.56 4
rs8126001
RGS19 ; OPRL1
20 64080106 5 prime UTR variant C/T snv 0.46 4
rs900399
LINC02029
3 157080943 upstream gene variant A/G snv 0.36 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs10049088
LINC02029
3 157079859 upstream gene variant C/T snv 0.35 3
rs10245353 7 25818994 intergenic variant C/A snv 0.16 3
rs10761785
REEP3
10 63559006 intron variant G/T snv 0.51 3
rs10923724 1 119004219 upstream gene variant C/T snv 0.53 3
rs10980797
LOC105376219
9 111150273 intron variant A/G;T snv 3
rs1106529
TBX15
1 118988874 intron variant G/A snv 0.77 3