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: rs10402271
rs10402271 		7 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs1048699
rs1048699
MARK4 ; PPP1R37
2 1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs11136000
rs11136000
CLU
19 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.700 1.000 1 2009 2009
dbSNP: rs1114832
rs1114832
MARK4 ; PPP1R37
2 1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs11894266
rs11894266 		2 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs12518099
rs12518099
LINC01339
3 0.925 0.120 5 90250292 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs12610605
rs12610605
NECTIN2
2 1.000 0.080 19 44867581 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
23 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 0.700 1.000 1 2009 2009
dbSNP: rs157580
rs157580
TOMM40
14 0.882 0.160 19 44892009 intron variant G/A snv 0.69 0.700 1.000 1 2009 2009
dbSNP: rs1871047
rs1871047
NECTIN2
2 1.000 0.080 19 44848489 intron variant A/G snv 0.31 0.700 1.000 1 2009 2009
dbSNP: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2009 2009
dbSNP: rs2582367
rs2582367 		2 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 0.700 1.000 1 2009 2009
dbSNP: rs2927438
rs2927438 		6 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs2943641
rs2943641 		18 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 0.700 1.000 1 2009 2009
dbSNP: rs2965101
rs2965101 		6 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs3760627
rs3760627
CLPTM1
2 1.000 0.080 19 44953923 non coding transcript exon variant T/C snv 0.80 0.51 0.700 1.000 1 2009 2009
dbSNP: rs377702
rs377702
NECTIN2
2 1.000 0.080 19 44859410 intron variant G/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs3851179
rs3851179 		15 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 0.700 1.000 1 2009 2009
dbSNP: rs405509
rs405509
APOE
30 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs439401
rs439401 		8 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 0.700 1.000 1 2009 2009
dbSNP: rs4689388
rs4689388
WFS1
4 0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 0.700 1.000 1 2009 2009
dbSNP: rs4712523
rs4712523
CDKAL1
3 0.925 0.120 6 20657333 intron variant A/G snv 0.41 0.700 1.000 1 2009 2009
dbSNP: rs5167
rs5167
APOC2 ; APOC4 ; APOC4-APOC2
7 1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 0.700 1.000 1 2009 2009
dbSNP: rs543293
rs543293 		3 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs6859
rs6859
NECTIN2
10 0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 0.700 1.000 1 2009 2009