Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 6