Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012657750
SELENBP1
1 151368294 missense variant G/C snv 2
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs10488698
BUD13
1.000 0.040 11 116763231 missense variant G/A snv 6.4E-02 4.8E-02 2
rs10488699
BUD13
11 116761784 intron variant C/T snv 1.0E-01 1
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1057519655
LDLR
1.000 0.080 19 11105516 missense variant T/C;G snv 4.0E-06 2
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10892151
DSCAML1 ; LOC105369515
1.000 11 117661016 intron variant C/T snv 9.7E-02 3
rs11039155
NR1H3
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12 6
rs11066782
KCTD10
1.000 0.040 12 109472747 intron variant C/T snv 0.17 2
rs11067233
MMAB
1.000 0.040 12 109556403 3 prime UTR variant C/G snv 0.23 0.24 2
rs1121923
LPL
8 19951924 synonymous variant G/A snv 3.3E-02 5.6E-02 1
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11542035
APOE
19 44908706 missense variant G/A snv 1.9E-05 2.8E-05 1
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs11613718
KCTD10
1.000 0.040 12 109474527 intron variant C/T snv 0.17 2
rs11774572 1.000 0.040 8 11589291 regulatory region variant C/G;T snv 2
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs11961407
CCHCR1
6 31154630 missense variant G/A snv 3.0E-03 1.3E-02 2
rs1211098985
MTRR
1.000 0.040 5 7878128 missense variant T/C;G snv 4.0E-06 3
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs12363280
SIRT3
11 231980 intron variant C/A;G snv 1
rs1249051329
SELENBP1
1 151369834 synonymous variant T/C snv 3.5E-05 2