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: rs1573649
rs1573649
1 1.000 0.120 6 32763481 5 prime UTR variant G/A;C snv 0.56 0.700 1.000 1 2007 2007
dbSNP: rs2051549
rs2051549
4 0.851 0.280 6 32762309 intron variant G/A snv 0.64 0.700 1.000 1 2007 2007
dbSNP: rs2071550
rs2071550
1 1.000 0.120 6 32763163 intron variant C/A snv 0.30 0.700 1.000 1 2007 2007
dbSNP: rs2301271
rs2301271
3 0.882 0.240 6 32757416 intron variant A/G snv 0.60 0.700 1.000 1 2007 2007
dbSNP: rs6903130
rs6903130
3 0.882 0.200 6 32764433 upstream gene variant G/A snv 0.53 0.700 1.000 1 2007 2007
dbSNP: rs7453920
rs7453920
5 0.752 0.440 6 32762235 intron variant A/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs7756516
rs7756516
3 0.851 0.280 6 32756140 3 prime UTR variant C/T snv 0.49 0.700 1.000 1 2007 2007