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: rs1137100
rs1137100
20 0.692 0.464 1 65570758 missense variant A/G snp 0.30 0.28 0.010 < 0.001 1 2012 2012
dbSNP: rs1137101
rs1137101
41 0.605 0.679 1 65592830 missense variant A/G snp 0.51 0.53 0.010 < 0.001 1 2012 2012
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: rs2881766
rs2881766
4 0.846 0.071 6 151797984 intron variant T/G snp 0.35 0.010 1.000 1 2015 2015
dbSNP: rs3104746
rs3104746
3 0.878 0.071 16 52567188 intron variant T/A snp 8.7E-02 0.010 1.000 1 2014 2014
dbSNP: rs3803662
rs3803662
13 0.724 0.250 16 52552429 non coding transcript exon variant A/G snp 0.62 0.010 1.000 1 2013 2013
dbSNP: rs6099128
rs6099128
3 0.878 0.071 20 56390288 intron variant T/G snp 0.13 0.010 1.000 1 2016 2016
dbSNP: rs926778
rs926778
4 0.846 0.071 6 152034647 intron variant C/A snp 0.40 0.010 1.000 1 2015 2015