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: rs17109512
rs17109512
LOC105378449
1 10 98367794 intergenic variant G/A snp 9.1E-02 0.800 1 2011 2011
dbSNP: rs10096633
rs10096633 		7 1.000 0.036 8 19973410 intergenic variant C/T snp 0.20 0.700 1 2011 2011
dbSNP: rs10198552
rs10198552
ACMSD
2 2 134842306 intron variant T/C snp 6.0E-02 0.700 1 2013 2013
dbSNP: rs10199768
rs10199768
APOB
4 2 21021128 intron variant G/T snp 0.34 0.700 1 2011 2011
dbSNP: rs10468017
rs10468017
LOC101928635
12 0.846 0.107 15 58386313 intron variant C/T snp 0.25 0.700 1 2011 2011
dbSNP: rs1047964
rs1047964
BACE1 ; RNF214
3 11 117286177 3 prime UTR variant G/A,C,T snp 6.1E-04; 5.6E-02; 6.7E-03 0.700 1 2011 2011
dbSNP: rs10503669
rs10503669 		6 1.000 0.036 8 19990179 intergenic variant C/A snp 8.2E-02 0.700 1 2011 2011
dbSNP: rs11076175
rs11076175
CETP
5 16 56972466 intron variant A/G snp 0.19 0.700 1 2011 2011
dbSNP: rs11508026
rs11508026
CETP
7 16 56965416 intron variant C/T snp 0.33 0.700 1 2011 2011
dbSNP: rs1169288
rs1169288
HNF1A
13 0.821 0.143 12 120978847 missense variant A/C,T snp 0.35 0.29; 3.2E-05 0.700 1 2011 2011
dbSNP: rs1169310
rs1169310
HNF1A
2 12 121001630 3 prime UTR variant G/A snp 0.31 0.700 1 2011 2011
dbSNP: rs1169313
rs1169313
C12orf43
4 12 121004867 intron variant T/A,C snp 3.2E-05; 0.31 0.700 1 2011 2011
dbSNP: rs11722228
rs11722228
SLC2A9
2 4 9914117 intron variant C/T snp 0.32 0.700 1 2011 2011
dbSNP: rs11754288
rs11754288
SLC17A1 ; SLC17A4
2 6 25776721 missense variant G/A snp 0.36 0.31 0.700 1 2011 2011
dbSNP: rs1183910
rs1183910
HNF1A
5 1.000 0.071 12 120983004 intron variant G/A snp 0.28 0.700 1 2011 2011
dbSNP: rs11986942
rs11986942 		3 8 20009934 intergenic variant C/G,T snp 0.39 0.700 1 2011 2011
dbSNP: rs1260326
rs1260326
GCKR
63 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2011 2011
dbSNP: rs12678919
rs12678919 		8 0.923 0.071 8 19986711 intergenic variant A/G snp 9.7E-02 0.700 1 2011 2011
dbSNP: rs12679834
rs12679834
LPL
5 8 19962922 intron variant T/C snp 9.1E-02 0.700 1 2011 2011
dbSNP: rs12708967
rs12708967 		4 16 56959299 intergenic variant T/C snp 0.17 0.700 1 2011 2011
dbSNP: rs12721109
rs12721109
APOC4 ; APOC4-APOC2
3 19 44943964 intron variant G/A snp 1.6E-02 0.700 1 2011 2011
dbSNP: rs12740374
rs12740374
CELSR2
10 0.878 0.036 1 109274968 3 prime UTR variant G/T snp 0.22 0.700 1 2011 2011
dbSNP: rs13077101
rs13077101
RABL3
3 3 120706484 intron variant T/C snp 0.24 0.700 1 2013 2013
dbSNP: rs13129697
rs13129697
SLC2A9
3 1.000 0.107 4 9925343 intron variant T/G snp 0.37 0.700 1 2011 2011
dbSNP: rs1333049
rs1333049 		30 0.715 0.286 9 22125504 intergenic variant G/C snp 0.41 0.700 1 2011 2011