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: rs1803274
rs1803274
BCHE
13 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.800 1.000 2 2011 2011
dbSNP: rs11675251
rs11675251
ABI2
1 2 203384676 intron variant A/G snv 0.44 0.800 1.000 1 2011 2011
dbSNP: rs4950806
rs4950806
RNPEP
1 1 201983446 5 prime UTR variant T/C snv 0.58 0.60 0.800 1.000 1 2011 2011
dbSNP: rs10049010
rs10049010 		1 3 165771709 intron variant T/C snv 8.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs10049434
rs10049434 		1 3 165771245 intron variant G/C snv 8.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs10049436
rs10049436 		2 1.000 0.080 3 165771478 intron variant C/T snv 8.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs1007845
rs1007845 		1 3 165722308 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10096633
rs10096633 		8 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs10199768
rs10199768
APOB
5 2 21021128 intron variant G/T snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs10211196
rs10211196
CYP20A1
1 2 203265173 intron variant G/A snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs1036584
rs1036584 		1 3 165897353 regulatory region variant C/G snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs1036585
rs1036585 		1 3 165906046 intergenic variant A/G snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs10439267
rs10439267
NBEAL1
1 2 203058724 intron variant C/T snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs10468017
rs10468017
ALDH1A2
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs1047964
rs1047964
BACE1 ; RNF214
3 11 117286177 3 prime UTR variant G/A;C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10497870
rs10497870
NBEAL1
2 2 203105560 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10503669
rs10503669 		8 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs10513616
rs10513616 		1 3 165749249 intron variant A/G snv 9.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs10513619
rs10513619 		1 3 165697049 intron variant G/A snv 8.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs10513621
rs10513621 		1 3 166009331 intergenic variant T/G snv 9.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs10513622
rs10513622 		1 3 166009461 intergenic variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10800805
rs10800805
RNPEP ; LOC112268254
1 1 201990610 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10936458
rs10936458 		1 3 165867467 intergenic variant C/T snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs10936468
rs10936468 		1 3 166041120 intergenic variant A/G snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs10936474
rs10936474 		1 3 166207739 intergenic variant G/T snv 0.58 0.700 1.000 1 2011 2011