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: rs10759102
rs10759102
PTPRD
1 9 9910123 intron variant G/A snv 0.38 0.800 1.000 1 2012 2012
dbSNP: rs12905014
rs12905014 		1 15 92340610 intergenic variant T/C snv 2.4E-02 0.800 1.000 1 2012 2012
dbSNP: rs13144621
rs13144621 		1 4 108296773 intergenic variant T/C snv 0.62 0.800 1.000 1 2012 2012
dbSNP: rs16889038
rs16889038
DCDC2
1 6 24306159 intron variant T/G snv 0.11 0.800 1.000 1 2012 2012
dbSNP: rs17486278
rs17486278
CHRNA5
9 0.827 0.120 15 78575140 intron variant A/C snv 0.32 0.800 1.000 1 2012 2012
dbSNP: rs181654
rs181654 		1 10 117620145 intergenic variant A/G snv 0.62 0.800 1.000 1 2012 2012
dbSNP: rs1997352
rs1997352
RARB
1 3 25496826 intron variant C/A;T snv 0.800 1.000 1 2012 2012
dbSNP: rs2044029
rs2044029
THSD4
1 15 71387620 intron variant A/G snv 0.61 0.800 1.000 1 2012 2012
dbSNP: rs4534959
rs4534959
LINC01924 ; LINC01538
1 18 64209921 intron variant A/G snv 4.2E-02 0.800 1.000 1 2012 2012
dbSNP: rs4767234
rs4767234 		1 12 114200043 intergenic variant A/C;T snv 0.800 1.000 1 2012 2012
dbSNP: rs6684428
rs6684428
LINC01755
1 1 55894140 intron variant T/A snv 0.17 0.800 1.000 1 2012 2012
dbSNP: rs715921
rs715921
SPATA13
1 13 24221351 intron variant G/A snv 0.28 0.800 1.000 1 2012 2012
dbSNP: rs7733088
rs7733088
HTR4 ; LOC107986462
5 1.000 0.040 5 148476770 intron variant G/A;C snv 0.44; 4.1E-06 0.800 1.000 1 2012 2012
dbSNP: rs8031948
rs8031948
HYKK
5 1.000 0.040 15 78523715 intron variant G/T snv 0.27 0.800 1.000 1 2012 2012
dbSNP: rs9536318
rs9536318 		1 13 52920559 intergenic variant G/A snv 0.81 0.800 1.000 1 2012 2012
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 3 2010 2012
dbSNP: rs1036429
rs1036429
SNRPF ; CCDC38
4 12 95877650 intron variant T/C snv 0.79 0.700 1.000 2 2011 2012
dbSNP: rs11001819
rs11001819
LRMDA
4 10 76555466 intron variant G/A snv 0.41 0.700 1.000 2 2011 2012
dbSNP: rs11168048
rs11168048
HTR4 ; LOC107986462
4 5 148462790 intron variant T/C snv 0.38 0.700 1.000 2 2010 2012
dbSNP: rs12447804
rs12447804
MMP15
4 16 58041378 intron variant C/T snv 0.18 0.700 1.000 2 2011 2012
dbSNP: rs12477314
rs12477314 		4 2 238955452 regulatory region variant C/G;T snv 0.700 1.000 2 2011 2012
dbSNP: rs12899618
rs12899618
THSD4
4 15 71352781 intron variant G/A snv 0.14 0.700 1.000 2 2010 2012
dbSNP: rs1529672
rs1529672
RARB
6 1.000 0.040 3 25479091 intron variant C/A;T snv 0.700 1.000 2 2011 2012
dbSNP: rs16909898
rs16909898
PTCH1 ; LOC100507346
4 9 95468726 intron variant A/G snv 8.4E-02 0.10 0.700 1.000 2 2010 2012
dbSNP: rs1928168
rs1928168
CASC15
4 6 22017509 intron variant T/C snv 0.36 0.700 1.000 2 2011 2012