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: rs2517713
rs2517713
2 1.000 0.107 6 29950322 intron variant G/A,T snp 0.64 0.800 3 2009 2013
dbSNP: rs1412829
rs1412829
8 0.801 0.321 9 22043927 intron variant A/G snp 0.30 0.800 2 2010 2016
dbSNP: rs189897
rs189897
1 3 37477054 intron variant T/A snp 0.13 0.800 2 2010 2010
dbSNP: rs28421666
rs28421666
1 6 32624960 intergenic variant A/G snp 7.2E-02 0.800 2 2010 2017
dbSNP: rs2860580
rs2860580
1 6 29938914 A/C,G,T snp 1.6E-03; 0.58 0.800 2 2010 2017
dbSNP: rs2894207
rs2894207
4 0.923 0.036 6 31295974 intron variant T/C snp 0.20 0.800 2 2010 2017
dbSNP: rs29232
rs29232
3 0.923 0.214 6 29643654 intergenic variant C/T snp 0.35 0.800 2 2009 2010
dbSNP: rs3129055
rs3129055
2 1.000 0.107 6 29702484 regulatory region variant A/G snp 0.24 0.800 2 2009 2010
dbSNP: rs31489
rs31489
10 0.769 0.214 5 1342599 intron variant C/A snp 0.42 0.800 2 2010 2016
dbSNP: rs401681
rs401681
22 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.800 2 2010 2017
dbSNP: rs4977756
rs4977756
16 0.734 0.357 9 22068653 intron variant G/A snp 0.64 0.800 2 2010 2016
dbSNP: rs6774494
rs6774494
4 0.878 0.143 3 169364845 intron variant G/A snp 0.42 0.800 2 2010 2016
dbSNP: rs9510787
rs9510787
2 1.000 0.107 13 23631056 intron variant A/G snp 0.22 0.800 2 2010 2016
dbSNP: rs1572072
rs1572072
1 13 23553071 intergenic variant G/T snp 0.36 0.800 1 2010 2010
dbSNP: rs3869062
rs3869062
2 1.000 0.107 6 29967114 intron variant A/G snp 5.9E-02 0.700 3 2009 2013
dbSNP: rs5009448
rs5009448
1 6 29972711 intron variant T/C snp 0.73 0.700 3 2009 2013
dbSNP: rs9260734
rs9260734
1 6 29964889 intron variant G/A snp 0.21 0.700 3 2009 2013
dbSNP: rs29230
rs29230
4 0.878 0.250 6 29608616 missense variant A/C,G snp 4.1E-06; 0.18 0.15 0.700 2 2010 2013
dbSNP: rs3131866
rs3131866
1 6 29703963 intergenic variant G/A snp 0.24 0.700 2 2009 2010
dbSNP: rs417162
rs417162
1 6 29948728 3 prime UTR variant C/T snp 0.65 0.700 2 2009 2013
dbSNP: rs10163267
rs10163267
1 16 83940313 intron variant G/A,C snp 0.30 0.700 1 2013 2013
dbSNP: rs1016343
rs1016343
3 0.923 0.071 8 127081052 non coding transcript exon variant C/T snp 0.21 0.700 1 2010 2010
dbSNP: rs10411210
rs10411210
4 0.878 0.071 19 33041394 intron variant C/T snp 0.20 0.700 1 2010 2010
dbSNP: rs104886003
rs104886003
52 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 0.700 1 2016 2016
dbSNP: rs104894229
rs104894229
31 0.634 0.500 11 534289 missense variant C/A,G,T snp 0.700 1 2016 2016