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: rs342293
rs342293
2 7 106731773 intron variant C/G snp 0.43 0.800 6 2009 2017
dbSNP: rs7961894
rs7961894
2 12 121927677 intron variant C/T snp 7.0E-02 0.800 5 2009 2014
dbSNP: rs10914144
rs10914144
3 1 171980610 intron variant T/C snp 0.77 0.800 4 2009 2014
dbSNP: rs11071720
rs11071720
4 15 63049797 intron variant T/C,G snp 0.58 0.800 3 2009 2017
dbSNP: rs12485738
rs12485738
1 3 56831748 intron variant A/G snp 0.65 0.800 3 2009 2012
dbSNP: rs1354034
rs1354034
5 3 56815721 intron variant T/C snp 0.52 0.800 3 2011 2017
dbSNP: rs2138852
rs2138852
1 17 29376331 intron variant C/G,T snp 0.64 0.800 3 2009 2012
dbSNP: rs10506328
rs10506328
1 12 54293448 intron variant A/C snp 0.76 0.800 2 2009 2014
dbSNP: rs10876550
rs10876550
1 12 54318524 intron variant G/A snp 0.68 0.800 2 2011 2014
dbSNP: rs11602954
rs11602954
2 11 202856 intron variant G/A snp 0.18 0.800 2 2009 2012
dbSNP: rs1172130
rs1172130
3 1 205275825 intergenic variant G/A snp 0.31 0.800 2 2011 2014
dbSNP: rs11734132
rs11734132
1 4 6889792 intergenic variant G/C snp 0.18 0.800 2 2011 2014
dbSNP: rs1668873
rs1668873
3 1 205266862 intron variant G/A snp 0.28 0.800 2 2009 2012
dbSNP: rs2015599
rs2015599
2 12 29282547 intron variant G/A snp 0.51 0.800 2 2011 2017
dbSNP: rs2393967
rs2393967
2 10 63373396 intron variant A/C snp 0.23 0.800 2 2009 2012
dbSNP: rs6136489
rs6136489
3 20 1943088 intergenic variant T/G snp 0.44; 3.2E-05 0.800 2 2009 2012
dbSNP: rs647316
rs647316
1 2 31241963 intron variant A/G snp 0.79 0.800 2 2009 2012
dbSNP: rs7075195
rs7075195
1 10 63290899 intron variant A/G snp 0.38 0.800 2 2011 2014
dbSNP: rs8076739
rs8076739
1 17 29387569 intron variant C/T snp 0.64 0.800 2 2011 2014
dbSNP: rs8109288
rs8109288
2 19 16074749 non coding transcript exon variant G/A snp 3.5E-02 0.800 2 2011 2012
dbSNP: rs893001
rs893001
1 18 69849610 intron variant A/C snp 6.2E-02 0.800 2 2009 2012
dbSNP: rs10076782
rs10076782
1 5 159177955 intron variant G/A snp 0.39 0.800 1 2011 2011
dbSNP: rs10512627
rs10512627
1 3 124621375 intron variant G/C snp 0.43 0.800 1 2011 2011
dbSNP: rs10813766
rs10813766
1 9 331490 intron variant T/G snp 0.64 0.800 1 2011 2011
dbSNP: rs11653144
rs11653144
1 17 29348208 regulatory region variant C/T snp 0.43 0.800 1 2012 2012