Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2297797
CYB561D1
1.000 0.040 1 109498058 3 prime UTR variant C/T snv 0.37 2
rs236318
BCAR3
1.000 0.040 1 93584664 intron variant C/G snv 0.79 2
rs2477432
RAP1A
1.000 0.040 1 111642655 intron variant T/A snv 0.52 2
rs3027001
CADM3-AS1 ; CADM3
1.000 0.040 1 159199673 intron variant C/G;T snv 2
rs302719
RERE-AS1 ; RERE
1.000 0.040 1 8430260 intron variant T/G snv 0.33 2
rs3101338
LOC105378797
1 72284670 intron variant C/A snv 0.82 2
rs3128341
NEGR1 ; LOC105378797
1 72284165 intron variant T/C snv 0.82 2
rs35771425 1.000 0.040 1 211436426 downstream gene variant T/C;G snv 2
rs407102
MYBPHL
1 109303656 intron variant C/T snv 0.68 2
rs41314284
STUM
1 226602300 3 prime UTR variant C/T snv 6.4E-02 2
rs6429422
SDCCAG8
1 243309499 intron variant T/A;C;G snv 2
rs6685859
DPYD
1.000 0.040 1 97357213 intron variant G/C snv 0.45 2
rs72694951 1.000 0.040 1 150146987 upstream gene variant C/T snv 0.11 2
rs80289781
MIR137HG ; DPYD
1.000 0.040 1 97980274 intron variant C/G;T snv 2
rs9441956 1.000 0.040 1 221783857 intergenic variant C/T snv 0.52 2
rs10218712
FOXO6
1 41366625 intron variant T/G snv 0.34 1
rs1026997
NEGR1
1 72050604 intron variant T/C snv 0.45 1
rs10493450 1 68807756 intron variant A/T snv 0.13 1
rs10779271
ESRRG
1 216659647 intron variant A/G snv 0.33 1
rs10798879
HCRTR1 ; PEF1
1 31631214 intron variant T/C snv 0.55 1
rs10798880
HCRTR1 ; PEF1
1 31631487 intron variant G/A;T snv 1
rs10798882
PEF1 ; PEF1-AS1
1 31642946 intron variant C/G snv 0.58 1
rs10858096
PSMA5
1 109424482 intron variant C/A snv 0.43 1
rs10874938
LOC101928219 ; LINC02607
1 95710380 intron variant A/T snv 0.34 1
rs10911301
NMNAT2
1 183313440 intron variant A/G snv 0.40 1