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
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
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
rs775144154
SLC19A1
0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs4149570
TNFRSF1A
0.752 0.360 12 6342424 upstream gene variant A/C;G;T snv 11
rs454886
APC
0.763 0.280 5 112810420 intron variant A/G snv 0.26 10
rs34743033
TYMSOS ; TYMS
0.776 0.200 18 657657 5 prime UTR variant GGCCTGCCTCCGTCCCGCCGCGCCACTTGGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCCC/CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG delins 8
rs4855883
APEH
0.851 0.080 3 49673881 upstream gene variant G/A;C snv 4
rs1629816
GHRL ; GHRLOS ; SEC13
0.851 0.080 3 10294607 non coding transcript exon variant G/A;C snv 4
rs2114358
PVT1 ; MIR1206
0.851 0.160 8 128008933 non coding transcript exon variant G/A;C snv 0.63 4
rs11081899
ZNF24
0.851 0.160 18 35344446 5 prime UTR variant G/A;C;T snv 4
rs3812265
CNOT4
0.925 0.040 7 135364052 missense variant C/G;T snv 0.27 3
rs12676482
IKBKB
0.882 0.120 8 42316559 intron variant G/A snv 0.12 3
rs375557
LOC105370174
0.882 0.080 13 41557730 intergenic variant G/A;C snv 3
rs151264360
TYMS ; ENOSF1
0.925 0.040 18 673444 3 prime UTR variant AAGTTA/-;AAGTTAAAGTTA delins 3
rs10505168
MIR2053 ; CSMD3
0.925 0.040 8 112643523 non coding transcript exon variant T/C snv 0.33 0.36 2
rs1110277
SLC23A2
0.925 0.080 20 4874036 synonymous variant A/G snv 0.34 0.43 2
rs4987219
SLC23A2
0.925 0.080 20 4884300 intron variant C/G;T snv 2