Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 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
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 11
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 8
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7