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: rs2046210
rs2046210
14 0.734 0.143 6 151627231 intergenic variant G/A snp 0.39 0.010 1.000 1 2016 2016
dbSNP: rs2881766
rs2881766
4 0.846 0.071 6 151797984 intron variant T/G snp 0.35 0.010 1.000 1 2015 2015
dbSNP: rs926778
rs926778
4 0.846 0.071 6 152034647 intron variant C/A snp 0.40 0.010 1.000 1 2015 2015
dbSNP: rs17879961
rs17879961
33 0.615 0.321 22 28725099 missense variant A/C,G snp 4.1E-03 1.1E-02 0.010 1.000 1 2012 2012
dbSNP: rs3116068
rs3116068
1 1.000 11 66337522 3 prime UTR variant C/T snp 0.19 0.010 1.000 1 2014 2014
dbSNP: rs1052566
rs1052566
1 1.000 11 66337723 missense variant G/A snp 0.30 0.22 0.010 < 0.001 1 2014 2014