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: rs9978142
rs9978142 		4 1.000 0.040 21 34279939 intron variant A/G;T snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs712046
rs712046
LOC107985068
3 17 36031260 regulatory region variant C/T snv 0.54 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: rs12447804
rs12447804
MMP15
4 16 58041378 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs12716852
rs12716852
WWOX
4 16 78154841 intron variant G/A snv 0.57 0.700 1.000 1 2011 2011
dbSNP: rs2865531
rs2865531
CFDP1
5 1.000 0.040 16 75356418 intron variant T/A snv 0.52 0.700 1.000 1 2011 2011
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: rs12899618
rs12899618
THSD4
4 15 71352781 intron variant G/A snv 0.14 0.700 1.000 1 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: 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: 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: 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: rs3867498
rs3867498
SNRPN ; SNHG14
3 15 24833640 intron variant G/A snv 0.14 0.700 1.000 1 2007 2007
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: rs8033889
rs8033889
THSD4
2 15 71387741 intron variant G/T snv 0.23 0.700 1.000 1 2014 2014
dbSNP: rs1036429
rs1036429
SNRPF ; CCDC38
4 12 95877650 intron variant T/C snv 0.79 0.700 1.000 1 2011 2011
dbSNP: rs11067283
rs11067283
LOC107984437
2 12 114758086 intron variant T/A snv 0.24 0.700 1.000 1 2010 2010