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: rs9271858
rs9271858
1 1.000 0.036 6 32627446 intergenic variant A/G snp 0.800 1 2013 2013
dbSNP: rs1518111
rs1518111
4 0.878 0.250 1 206771300 intron variant T/C snp 0.71 0.010 1.000 1 2016 2016
dbSNP: rs1554286
rs1554286
5 0.821 0.321 1 206770888 intron variant A/G,T snp 0.72 0.73 0.010 1.000 1 2016 2016
dbSNP: rs17549193
rs17549193
2 0.923 0.107 9 134887180 missense variant C/T snp 0.26 0.29 0.010 1.000 1 2016 2016
dbSNP: rs2103816
rs2103816
1 1.000 0.036 6 170366925 intron variant T/A snp 0.58 0.010 1.000 1 2012 2012
dbSNP: rs3024498
rs3024498
5 0.821 0.250 1 206768184 3 prime UTR variant T/C snp 0.20 0.010 1.000 1 2016 2016
dbSNP: rs9460106
rs9460106
1 1.000 0.036 6 170306872 intron variant T/C,G snp 0.33 0.010 1.000 1 2012 2012