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: rs796065354
rs796065354
9 0.801 0.107 6 151944320 missense variant A/G snp 0.020 1.000 2 2007 2007
dbSNP: rs10941679
rs10941679
7 0.784 0.107 5 44706396 intergenic variant A/G snp 0.25 0.010 1.000 1 2012 2012
dbSNP: rs1131532
rs1131532
1 1.000 0.071 3 172506513 missense variant A/C,G,T snp 2.1E-05; 0.65 0.70 0.010 1.000 1 2010 2010
dbSNP: rs1136201
rs1136201
8 0.769 0.179 17 39723335 missense variant A/G,T snp 0.20 0.19 0.010 1.000 1 2006 2006
dbSNP: rs13387042
rs13387042
10 0.769 0.179 2 217041109 intergenic variant A/G snp 0.44 0.010 1.000 1 2009 2009
dbSNP: rs1801201
rs1801201
8 0.769 0.179 17 39723332 missense variant A/C,G snp 4.0E-06; 4.9E-03 4.2E-03 0.010 1.000 1 2006 2006
dbSNP: rs28997576
rs28997576
8 0.784 0.143 2 214752454 missense variant C/G,T snp 1.5E-02 1.4E-02 0.010 1.000 1 2007 2007
dbSNP: rs744154
rs744154
7 0.801 0.214 16 13921224 intron variant G/C snp 0.23 0.010 1.000 1 2009 2009
dbSNP: rs758272654
rs758272654
28 0.667 0.536 20 58909201 synonymous variant T/C snp 4.0E-06 0.010 1.000 1 2008 2008