Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12673692
THSD7A
0.925 0.120 7 11528903 intron variant G/A snv 0.30 2
rs1473
PUM1
0.925 0.120 1 30940072 intron variant G/A snv 6.8E-02 2
rs1554606
IL6 ; IL6-AS1
0.925 0.120 7 22729088 intron variant T/A;G snv 2
rs17277372
DNM3
0.925 0.120 1 172218334 intron variant A/G snv 0.22 2
rs1800780
NOS3
0.925 0.120 7 151001791 intron variant A/G snv 0.58 0.56 2
rs2178950
TRPS1
0.925 0.120 8 115640791 intron variant G/C snv 0.51 2
rs2288377
LOC105369944 ; IGF1
0.925 0.080 12 102480984 intron variant A/G;T snv 2
rs2566752
WLS ; GNG12-AS1
1.000 0.080 1 68191014 intron variant T/A;C snv 2
rs28377268
LOC100507346 ; PTCH1
0.925 0.080 9 95462774 intron variant G/A;C;T snv 2
rs297325
SOX6
0.925 0.120 11 16368048 intron variant T/C;G snv 2
rs335170
PRDM6
0.925 0.120 5 123146549 intron variant A/C;G;T snv 2
rs3918181
NOS3
0.925 0.120 7 151004695 intron variant G/A snv 0.35 2
rs4756846
SOX6
0.925 0.120 11 16381965 intron variant T/C snv 8.8E-02 2
rs4869739
CCDC170
1.000 0.080 6 151580667 intron variant A/T snv 0.44 2
rs491347
LRP5
0.925 0.200 11 68402220 intron variant G/A;T snv 2
rs6873545
GHR
0.925 0.200 5 42631162 intron variant T/C snv 0.31 2
rs6993813
COLEC10
1.000 0.080 8 119039999 intron variant T/C snv 0.60 2
rs7117858
LOC102724957
1.000 0.080 11 15672916 intron variant G/A;C snv 2
rs7605378
FTCDNL1
0.925 0.120 2 199812203 intron variant A/C snv 0.64 2
rs784288
MECOM
1.000 0.080 3 169253443 intron variant A/G;T snv 2
rs9825174
XXYLT1
0.925 0.120 3 195118855 intron variant C/A;G;T snv 2
rs10203122
FTCDNL1
1.000 0.080 2 199831723 intron variant T/C snv 0.16 1
rs10832915
SAA1
1.000 0.080 11 18269516 intron variant T/C;G snv 1
rs11872467
RAB31
1.000 0.080 18 9848005 intron variant G/A snv 3.4E-02 1
rs1256044
ESR2
1.000 0.080 14 64267309 intron variant G/A snv 0.66 1