Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 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
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
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
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
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 8
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 7
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 7