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: rs12504628
rs12504628
6 1.000 0.040 4 144515172 intron variant T/C snv 0.33 0.700 1.000 3 2009 2010
dbSNP: rs1032297
rs1032297
4 4 144513592 intron variant A/G snv 0.33 0.700 1.000 2 2009 2010
dbSNP: rs10516526
rs10516526
4 4 105767747 intron variant A/G snv 5.4E-02 0.700 1.000 2 2010 2010
dbSNP: rs11100860
rs11100860
4 4 144557987 intron variant A/G snv 0.43 0.700 1.000 2 2009 2010
dbSNP: rs11938745
rs11938745
4 4 144544616 intron variant T/C snv 0.32 0.700 1.000 2 2009 2010
dbSNP: rs12509311
rs12509311
4 4 144557510 intron variant C/T snv 0.31 0.700 1.000 2 2009 2010
dbSNP: rs12511230
rs12511230
4 4 144550093 intron variant A/T snv 0.33 0.700 1.000 2 2009 2010
dbSNP: rs13141641
rs13141641
8 1.000 0.040 4 144585304 intron variant T/C snv 0.32 0.700 1.000 2 2009 2010
dbSNP: rs13147758
rs13147758
5 4 144539078 intron variant A/G snv 0.31 0.700 1.000 2 2009 2010
dbSNP: rs13148031
rs13148031
4 4 144539186 intron variant A/G snv 0.33 0.700 1.000 2 2009 2010
dbSNP: rs1489759
rs1489759
7 0.882 0.080 4 144553321 intron variant A/G snv 0.43 0.700 1.000 2 2009 2010
dbSNP: rs1489762
rs1489762
4 4 144533812 intron variant T/C;G snv 0.700 1.000 2 2009 2010
dbSNP: rs1512281
rs1512281
4 4 144513749 intron variant A/G snv 0.32 0.700 1.000 2 2009 2010
dbSNP: rs1512288
rs1512288
5 1.000 0.040 4 144570129 intron variant G/A snv 0.42 0.700 1.000 2 2009 2010
dbSNP: rs1828591
rs1828591
5 1.000 0.040 4 144559628 intron variant A/G snv 0.43 0.700 1.000 2 2009 2010
dbSNP: rs1980057
rs1980057
6 1.000 0.040 4 144564586 intron variant C/T snv 0.31 0.700 1.000 2 2009 2010
dbSNP: rs2070600
rs2070600
82 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.700 1.000 2 2010 2010
dbSNP: rs2130339
rs2130339
4 4 144543733 intron variant A/G snv 0.43 0.700 1.000 2 2009 2010
dbSNP: rs4331881
rs4331881
2 5 157517467 intron variant G/T snv 0.42 0.700 1.000 2 2010 2010
dbSNP: rs6537292
rs6537292
4 4 144548816 intron variant G/T snv 0.32 0.700 1.000 2 2009 2010
dbSNP: rs6537296
rs6537296
4 4 144566782 intron variant A/G snv 0.37 0.700 1.000 2 2009 2010
dbSNP: rs6817273
rs6817273
5 1.000 0.040 4 144570851 intron variant T/A;C snv 0.33 0.700 1.000 2 2009 2010
dbSNP: rs6828540
rs6828540
4 4 144542079 intron variant G/A;C snv 0.700 1.000 2 2009 2010
dbSNP: rs6830832
rs6830832
4 4 144544339 intron variant T/G snv 0.44 0.700 1.000 2 2009 2010
dbSNP: rs6842889
rs6842889
4 4 144558728 intron variant T/C snv 0.33 0.700 1.000 2 2009 2010