Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs775144154
SLC19A1
0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs368087026
SLC19A1
0.637 0.520 21 45530890 missense variant G/A snv 33
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1359880314
SLC19A1
0.763 0.320 21 45534541 synonymous variant C/T snv 1.6E-05 2.8E-05 12
rs4705343
MIR143 ; CARMN
0.790 0.240 5 149428518 non coding transcript exon variant T/C snv 0.14 7
rs1465444723
TCN2
0.827 0.240 22 30610886 missense variant A/G snv 4.0E-06 5
rs121908601
ZFPM2
0.851 0.080 8 105419192 missense variant A/C;G snv 4.0E-06; 2.7E-03 4
rs187043152
ZFPM2 ; ZFPM2-AS1
0.851 0.080 8 105801714 missense variant G/A;T snv 3.4E-03; 4.0E-06 4
rs353292
MIR143 ; CARMN
0.882 0.080 5 149428245 non coding transcript exon variant G/A snv 0.35 3
rs3087465
TGFBR2 ; LOC105377015
1.000 3 30605668 upstream gene variant A/G;T snv 0.64 3
rs202204708
ZFPM2-AS1 ; ZFPM2
0.882 0.080 8 105788864 missense variant A/G snv 4.5E-04 4.7E-04 3
rs11017328 0.925 0.080 10 130548836 regulatory region variant C/G;T snv 2
rs1959122 0.925 0.080 14 81871321 intron variant C/A;T snv 2
rs6140038 0.925 0.080 20 6601515 intergenic variant C/A;T snv 2
rs6545278 0.925 0.080 2 52478914 upstream gene variant T/G snv 3.8E-02 2
rs1396258746
ADD1
0.925 0.120 4 2898474 missense variant G/C snv 4.0E-06 1.4E-05 2
rs2267386
LOC105373029 ; KCNJ4
0.925 0.080 22 38436107 intron variant G/A snv 2.7E-02 2
rs6763159
LOC105377110
0.925 0.080 3 59663795 intron variant T/C snv 0.52 2