Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13023094
SLC4A1AP
0.925 0.120 2 27687839 intron variant A/C snv 0.16 4
rs1124511
EDEM2 ; MMP24-AS1-EDEM2
20 35148894 upstream gene variant A/C snv 0.48 2
rs11696967
MMP24-AS1-EDEM2
20 35155806 intergenic variant A/C snv 0.23 2
rs12621149
IWS1
2 127509268 intron variant A/C snv 0.68 2
rs17362834
EPB41L1 ; LOC100130373
20 36147283 intron variant A/C snv 2.8E-02 2
rs2268081
RALY
20 34016024 intron variant A/C snv 8.7E-02 2
rs2295097
ACSS2
20 34890418 intron variant A/C snv 5.9E-02 2
rs2425024
MMP24-AS1-EDEM2 ; MMP24 ; MMP24OS
20 35257135 intron variant A/C snv 0.34 2
rs4911495
UQCC1
20 35384175 intron variant A/C snv 8.5E-02 6.1E-02 2
rs6088721
EDEM2 ; MMP24-AS1-EDEM2
20 35118208 intron variant A/C snv 0.60 2
rs6121021
CPNE1 ; RBM12
20 35664516 5 prime UTR variant A/C snv 6.7E-02 2
rs6121022 20 35667085 intron variant A/C snv 6.7E-02 2
rs6121023
NFS1
20 35668718 3 prime UTR variant A/C snv 6.7E-02 2
rs6430936 2 127250110 downstream gene variant A/C snv 0.77 2
rs7568070
CYP27C1
2 127195478 synonymous variant A/C snv 0.26 0.32 2
rs819156
AHCY
20 34293217 intron variant A/C snv 0.87 2
rs882436
FER1L4
20 35607349 intron variant A/C snv 0.10 2
rs11700080
ITCH
20 34458956 intron variant A/C;G snv 2
rs12477670
MYO7B
2 127576951 intron variant A/C;G snv 2
rs13038810 20 36282301 intergenic variant A/C;G snv 2
rs17336615
NFS1
20 35674089 non coding transcript exon variant A/C;G snv 2
rs17406518
MMP24OS ; MMP24-AS1-EDEM2 ; PROCR
20 35211373 intron variant A/C;G snv 2
rs224332
GDF5-AS1 ; GDF5
20 35434874 missense variant A/C;G snv 2
rs6060172
TRPC4AP
20 35041002 intron variant A/C;G snv 2
rs6060546
NFS1
20 35669741 intron variant A/C;G snv 2