Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11075253
rs11075253
PDXDC1 ; NTAN1
1 16 15054789 intron variant C/A snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs115136538
rs115136538
ADAMTS3
1 4 72456848 intron variant T/C snv 5.7E-03 0.800 1.000 1 2012 2012
dbSNP: rs115849089
rs115849089 		7 8 20054859 intergenic variant G/A snv 9.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs1168029
rs1168029
DOCK7
1 1 62503731 intron variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs13247874
rs13247874
MLXIPL
1 7 73596112 intron variant C/T snv 0.15 0.15 0.800 1.000 1 2012 2012
dbSNP: rs2575876
rs2575876
ABCA1
7 9 104903458 intron variant G/A snv 0.24 0.800 1.000 1 2012 2012
dbSNP: rs35853021
rs35853021
ALDH1A2
1 15 58388444 intron variant G/T snv 0.38 0.800 1.000 1 2012 2012
dbSNP: rs3764261
rs3764261 		26 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.800 1.000 1 2012 2012
dbSNP: rs55791371
rs55791371
SMARCA4
3 0.925 0.080 19 11077477 intron variant A/C snv 0.11 0.800 1.000 1 2012 2012
dbSNP: rs651821
rs651821
APOA5
17 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 0.800 1.000 1 2012 2012
dbSNP: rs67418890
rs67418890 		1 1 161571067 intron variant T/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs6917603
rs6917603
ZNRD1ASP
2 6 30049294 intron variant T/C snv 0.15 0.800 1.000 1 2012 2012
dbSNP: rs7228085
rs7228085
LOC105372112
1 18 49634444 intergenic variant A/G snv 0.53 0.800 1.000 1 2012 2012
dbSNP: rs72669744
rs72669744 		1 1 55650832 intron variant C/T snv 2.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs7412
rs7412
APOE
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.800 1.000 1 2012 2012
dbSNP: rs1059611
rs1059611
LPL
3 8 19967052 3 prime UTR variant T/C snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs10889353
rs10889353
DOCK7
5 1 62652525 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1160985
rs1160985
TOMM40
6 1.000 0.080 19 44900155 intron variant C/T snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs11644601
rs11644601
PDXDC1 ; RRN3
4 16 15078261 intron variant T/C snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs1167998
rs1167998
DOCK7
6 1 62465961 intron variant C/A snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs1168041
rs1168041
DOCK7
2 1 62494579 non coding transcript exon variant T/C snv 0.61 0.700 1.000 1 2016 2016
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2009 2009
dbSNP: rs12713956
rs12713956
APOB
4 2 21018633 intron variant A/G snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs1367117
rs1367117
APOB
8 1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 0.700 1.000 1 2009 2009
dbSNP: rs1532085
rs1532085
ALDH1A2
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.700 1.000 1 2009 2009