Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 16
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 11
rs492602
LOC105447645 ; FUT2
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 7
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 5
rs2287921
RASIP1
1.000 0.040 19 48725015 non coding transcript exon variant T/C snv 0.37 4
rs3760776
FUT6
0.925 0.120 19 5839735 upstream gene variant G/A snv 0.22 3
rs708686
FUT6
19 5840608 upstream gene variant C/T snv 0.46 3
rs4654748
NBPF3
1.000 0.040 1 21459575 intron variant C/T snv 0.38 3
rs526934
TCN1
0.925 0.080 11 59866020 intron variant G/A snv 0.77 3
rs12085006 1 11898666 intergenic variant A/G;T snv 2
rs1256335
ALPL
1 21563893 intron variant G/A snv 0.80 2
rs11254363
CUBN
1.000 0.040 10 17088694 intron variant A/G snv 0.26 2
rs982393
FIGN
2 163634019 intron variant A/C;T snv 2
rs3760775
FUT6
19 5841345 upstream gene variant G/T snv 0.15 2
rs10986018
GABBR2
9 98361054 intron variant T/C snv 7.9E-02 2
rs34324219
TCN1
11 59855905 missense variant C/A snv 8.6E-02 9.0E-02 2
rs146226203 5 150806264 intergenic variant C/G snv 3.1E-03 1
rs41281112
CLYBL ; LOC101927437
13 99866380 stop gained C/T snv 2.8E-02 2.2E-02 1
rs9473555
MMUT
6 49441774 intron variant G/C snv 0.36 1
rs2298585
MS4A3
11 60069719 intron variant C/T snv 1.6E-02 2.3E-02 1
rs10515552
PRELID2
5 145659268 intron variant T/C snv 6.7E-02 1