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: rs10811661
rs10811661 		22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.800 1.000 5 2012 2015
dbSNP: rs2191349
rs2191349 		4 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 0.800 1.000 5 2010 2019
dbSNP: rs10885122
rs10885122 		4 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 0.800 1.000 4 2010 2019
dbSNP: rs1387153
rs1387153 		10 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 0.800 1.000 4 2009 2019
dbSNP: rs1483121
rs1483121 		4 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 0.800 1.000 3 2012 2019
dbSNP: rs895636
rs895636 		2 2 44961214 non coding transcript exon variant C/T snv 0.23 0.700 1.000 3 2011 2018
dbSNP: rs10830962
rs10830962 		7 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 0.700 1.000 2 2011 2019
dbSNP: rs1974620
rs1974620 		2 1.000 0.080 7 15025842 intergenic variant C/A;T snv 0.700 1.000 2 2015 2019
dbSNP: rs2166706
rs2166706 		2 1.000 0.080 11 92958366 intergenic variant T/A;C snv 0.800 1.000 2 2009 2019
dbSNP: rs3847554
rs3847554 		1 11 92935660 upstream gene variant C/T snv 0.56 0.700 1.000 2 2015 2019
dbSNP: rs7936247
rs7936247 		5 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 0.700 1.000 2 2013 2019
dbSNP: rs10228456
rs10228456 		3 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs10747083
rs10747083 		2 12 132465032 downstream gene variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11039130
rs11039130 		2 11 47207765 intergenic variant C/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs11041816
rs11041816 		2 11 8222251 downstream gene variant A/G snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs11071657
rs11071657 		3 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 0.700 1.000 1 2010 2010
dbSNP: rs11195502
rs11195502 		2 10 111279909 intergenic variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1120557
rs1120557 		1 14 62662722 regulatory region variant A/G snv 0.88 0.700 1.000 1 2009 2009
dbSNP: rs11257655
rs11257655 		4 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs11607883
rs11607883 		2 11 45818158 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs11782386
rs11782386 		2 8 9344277 intron variant C/T snv 9.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs118137427
rs118137427 		2 10 111217250 intergenic variant A/G snv 3.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs12385797
rs12385797 		1 11 106465562 upstream gene variant C/A snv 6.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs12440695
rs12440695 		3 15 62142957 regulatory region variant T/C snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs1280
rs1280 		2 3 170995501 intron variant T/C snv 0.20 0.700 1.000 1 2012 2012