Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs10748835
AS3MT ; LOC107984265 ; BORCS7-ASMT
0.827 0.160 10 102900499 non coding transcript exon variant G/A snv 0.41 5
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs879254840
LDLR ; MIR6886
0.827 0.120 19 11113322 missense variant A/G snv 5
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs1941404
NNMT
0.882 0.120 11 114298316 non coding transcript exon variant A/G snv 0.59 3
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs974389711
APOA1 ; APOA1-AS
1.000 0.040 11 116836210 synonymous variant C/T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs632793 0.882 0.120 1 11850620 upstream gene variant A/G snv 0.45 3
rs198388
NPPB
0.851 0.160 1 11857283 downstream gene variant C/G;T snv 4
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs2302685
BCL2L14 ; LRP6
0.827 0.240 12 12148964 missense variant C/T snv 0.85 0.84 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2222823
MYLK
0.925 0.080 3 123885940 upstream gene variant T/A snv 0.14 4
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs4757268
PDE3B
0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs200960801
ESR1
0.827 0.200 6 151944488 missense variant A/G snv 4.0E-06 6