Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10