Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070665
APOA1 ; APOA1-AS
11 116836968 intron variant A/C;G snv 0.85 2
rs632153
APOA1 ; APOA1-AS
11 116839523 intron variant G/C;T snv 2
rs5104
APOA4
11 116821618 missense variant C/T snv 0.80 0.85 2
rs1801701
APOB
1.000 0.080 2 21005955 missense variant C/T snv 7.0E-02 6.6E-02 2
rs10488698
BUD13
1.000 0.040 11 116763231 missense variant G/A snv 6.4E-02 4.8E-02 2
rs2187126
BUD13
11 116765068 intron variant A/G snv 4.8E-02 2
rs11961407
CCHCR1
6 31154630 missense variant G/A snv 3.0E-03 1.3E-02 2
rs78338345
GGA3
1.000 0.080 17 75242428 missense variant C/G snv 7.7E-03 2.5E-03 2
rs11066782
KCTD10
1.000 0.040 12 109472747 intron variant C/T snv 0.17 2
rs11613718
KCTD10
1.000 0.040 12 109474527 intron variant C/T snv 0.17 2
rs1057519655
LDLR
1.000 0.080 19 11105516 missense variant T/C;G snv 4.0E-06 2
rs3813627
MIR5187 ; APOA2 ; TOMM40L
1.000 0.080 1 161225358 upstream gene variant G/T snv 0.28 2
rs11067233
MMAB
1.000 0.040 12 109556403 3 prime UTR variant C/G snv 0.23 0.24 2
rs1012657750
SELENBP1
1 151368294 missense variant G/C snv 2
rs1249051329
SELENBP1
1 151369834 synonymous variant T/C snv 3.5E-05 2
rs771038258
SELENBP1
1 151365837 missense variant A/G snv 8.0E-06 2.1E-05 2
rs762304200
SHBG
17 7630716 synonymous variant A/G snv 2.8E-05 2
rs1289389
SLC15A1
13 98684036 3 prime UTR variant C/T snv 0.18 2
rs12953258
SOCS3 ; LOC101928674
1.000 0.080 17 78360015 5 prime UTR variant T/A;G snv 2
rs2472386
ABCA1
1.000 0.040 9 104839260 intron variant G/A snv 0.47 3
rs4646155
ACE2
0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02 3
rs4830542
ACE2
0.925 0.080 X 15558483 downstream gene variant C/G;T snv 3
rs512535
APOB
0.925 0.080 2 21044910 upstream gene variant T/C snv 0.45 3
rs10892151
DSCAML1 ; LOC105369515
1.000 11 117661016 intron variant C/T snv 9.7E-02 3
rs1746661
FNDC5
0.925 0.080 1 32869438 intron variant G/A;T snv 3