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: rs10824425
rs10824425 		2 10 76580552 intergenic variant G/C snv 0.42 0.700 1.000 1 2014 2014
dbSNP: rs11855326
rs11855326
THSD4
2 15 71318496 intron variant G/A snv 0.31 0.700 1.000 1 2014 2014
dbSNP: rs11858540
rs11858540
THSD4
2 15 71330447 intron variant T/G snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs12441227
rs12441227
THSD4
3 15 71404547 intron variant A/G snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs1441361
rs1441361
THSD4
2 15 71332783 intron variant A/G snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs17786786
rs17786786
THSD4
2 15 71316280 intron variant A/C snv 0.32 0.700 1.000 1 2014 2014
dbSNP: rs1837762
rs1837762
THSD4
2 15 71319964 intron variant G/A snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs2114719
rs2114719 		2 15 70640999 downstream gene variant A/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs2162555
rs2162555 		2 15 70641233 downstream gene variant T/C snv 0.85 0.700 1.000 1 2014 2014
dbSNP: rs2162556
rs2162556
LOC107984791
2 15 70644099 TF binding site variant T/C snv 0.85 0.700 1.000 1 2014 2014
dbSNP: rs2637260
rs2637260
LRMDA
2 10 76560588 intron variant T/C snv 0.53 0.700 1.000 1 2014 2014
dbSNP: rs2637261
rs2637261 		2 10 76560835 non coding transcript exon variant C/T snv 0.54 0.700 1.000 1 2014 2014
dbSNP: rs2637266
rs2637266 		2 10 76571560 intergenic variant A/G snv 0.48 0.700 1.000 1 2014 2014
dbSNP: rs6494886
rs6494886 		2 15 70641392 downstream gene variant A/C;T snv 0.700 1.000 1 2014 2014
dbSNP: rs6494904
rs6494904
THSD4
2 15 71317183 intron variant G/A snv 0.65 0.700 1.000 1 2014 2014
dbSNP: rs712046
rs712046
LOC107985068
3 17 36031260 regulatory region variant C/T snv 0.54 0.700 1.000 1 2014 2014
dbSNP: rs8033889
rs8033889
THSD4
2 15 71387741 intron variant G/T snv 0.23 0.700 1.000 1 2014 2014
dbSNP: rs854674
rs854674
LOC107985068
3 17 36032936 regulatory region variant T/C snv 0.57 0.700 1.000 1 2014 2014
dbSNP: rs854679
rs854679
LOC107985068
2 17 36031803 intergenic variant G/A;T snv 0.700 1.000 1 2014 2014
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
dbSNP: rs1036429
rs1036429
SNRPF ; CCDC38
4 12 95877650 intron variant T/C snv 0.79 0.700 1.000 1 2011 2011
dbSNP: rs11001819
rs11001819
LRMDA
4 10 76555466 intron variant G/A snv 0.41 0.700 1.000 1 2011 2011
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: rs12447804
rs12447804
MMP15
4 16 58041378 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs12477314
rs12477314 		4 2 238955452 regulatory region variant C/G;T snv 0.700 1.000 1 2011 2011