Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10748835
AS3MT ; LOC107984265 ; BORCS7-ASMT
0.827 0.160 10 102900499 non coding transcript exon variant G/A snv 0.41 5
rs121964971
CBS
0.851 0.160 21 43058215 missense variant G/A snv 1.2E-05 5
rs498005
HCN4
0.851 0.160 15 73327969 intron variant C/T snv 0.48 5
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs198388
NPPB
0.851 0.160 1 11857283 downstream gene variant C/G;T snv 4
rs4713518
TSBP1 ; TSBP1-AS1
0.925 0.160 6 32289560 intron variant A/G;T snv 3
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs3816873
MTTP
0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs573658040
APOE
0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 8
rs200960801
ESR1
0.827 0.200 6 151944488 missense variant A/G snv 4.0E-06 6
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs2302685
BCL2L14 ; LRP6
0.827 0.240 12 12148964 missense variant C/T snv 0.85 0.84 5
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33