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: rs2070600
rs2070600
AGER
82 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.700 1.000 2 2010 2010
dbSNP: rs12914385
rs12914385
CHRNA3
18 0.790 0.160 15 78606381 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2855812
rs2855812
MICB
13 0.790 0.360 6 31504943 intron variant G/T snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs6570507
rs6570507
ADGRG6
13 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 1 2010 2010
dbSNP: rs2036527
rs2036527 		12 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs2869967
rs2869967
FAM13A ; LOC105377327
11 0.827 0.120 4 88948181 intron variant T/C snv 0.49 0.700 1.000 1 2010 2010
dbSNP: rs11172113
rs11172113
LRP1
10 0.882 0.080 12 57133500 intron variant T/C snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs2571445
rs2571445
TNS1
10 0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 0.700 1.000 1 2010 2010
dbSNP: rs2857595
rs2857595 		9 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs2869966
rs2869966
FAM13A ; LOC105377327
9 1.000 0.040 4 88947927 intron variant C/T snv 0.47 0.700 1.000 1 2010 2010
dbSNP: rs13141641
rs13141641 		8 1.000 0.040 4 144585304 intron variant T/C snv 0.32 0.700 1.000 2 2009 2010
dbSNP: rs1489759
rs1489759
LOC105377462
7 0.882 0.080 4 144553321 intron variant A/G snv 0.43 0.700 1.000 2 2009 2010
dbSNP: rs7655625
rs7655625 		7 1.000 0.040 4 144564763 intron variant T/C;G snv 0.700 1.000 2 2009 2010
dbSNP: rs13118928
rs13118928 		7 0.925 0.040 4 144565237 intron variant A/G snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs7671167
rs7671167
FAM13A
7 0.925 0.040 4 88962828 intron variant C/T snv 0.53 0.700 1.000 1 2010 2010
dbSNP: rs12504628
rs12504628
LOC105377462
6 1.000 0.040 4 144515172 intron variant T/C snv 0.33 0.700 1.000 3 2009 2010
dbSNP: rs1980057
rs1980057 		6 1.000 0.040 4 144564586 intron variant C/T snv 0.31 0.700 1.000 2 2009 2010
dbSNP: rs1529672
rs1529672
RARB
6 1.000 0.040 3 25479091 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2284746
rs2284746
MFAP2
6 1 16980180 intron variant C/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs7741741
rs7741741
ADGRG6
6 0.925 0.040 6 142334664 intron variant T/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs13147758
rs13147758
LOC105377462
5 4 144539078 intron variant A/G snv 0.31 0.700 1.000 2 2009 2010
dbSNP: rs1512288
rs1512288 		5 1.000 0.040 4 144570129 intron variant G/A snv 0.42 0.700 1.000 2 2009 2010
dbSNP: rs1828591
rs1828591
LOC105377462
5 1.000 0.040 4 144559628 intron variant A/G snv 0.43 0.700 1.000 2 2009 2010
dbSNP: rs6817273
rs6817273 		5 1.000 0.040 4 144570851 intron variant T/A;C snv 0.33 0.700 1.000 2 2009 2010
dbSNP: rs7068966
rs7068966
CDC123
5 1.000 0.040 10 12235993 intron variant C/T snv 0.43 0.700 1.000 2 2010 2011