Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 18
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 14
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 12
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 12
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 10
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 8
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 7