Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200726463
PLCL2
3 16992491 intron variant -/AG delins 7.1E-03 1
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs112908525
CD36
7 80675962 intron variant -/GGGTTGAGA delins 0.38 3
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs66567989
TYMS
18 660442 intron variant A/- del 0.11 2
rs533649954
RAB11B-AS1
19 8387490 intron variant A/-;AA delins 3.0E-02 1
rs141007801
CASC15
6 21722558 intron variant A/-;AA;AAA;AAAA delins 2
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs138665726
UBE2L3
22 21563570 intron variant A/C snv 0.17 3
rs11078917 17 39590106 intergenic variant A/C snv 0.56 2
rs1578741 1 117716081 intergenic variant A/C snv 0.19 2
rs17700466 7 93006659 regulatory region variant A/C snv 0.12 2
rs2713936
TEX9
15 56253787 intron variant A/C snv 0.32 2
rs13011075 2 68412181 intergenic variant A/C snv 0.26 1
rs2923427
SLC20A2
8 42530605 intron variant A/C snv 0.55 1
rs34282584
SLC6A9
1 44022794 intron variant A/C snv 0.28 1
rs3893275
LOC105374303
3 196192085 regulatory region variant A/C snv 0.13 1
rs75085022
ZFAND4
10 45633821 intron variant A/C snv 6.1E-02 1
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs13091206
CCDC36
3 49201285 intron variant A/C;G snv 2
rs2145943 20 39934603 upstream gene variant A/C;G snv 2
rs3962382 1 67700010 downstream gene variant A/C;G snv 2
rs4238686
PIEZO1
16 88722526 non coding transcript exon variant A/C;G snv 2
rs7218708
SPECC1
17 20023523 intron variant A/C;G snv 2
rs79308158
RASA2
3 141529673 intron variant A/C;G snv 4.8E-02 2