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: rs3093024
rs3093024
3 0.882 0.200 6 167119305 non coding transcript exon variant A/G snv 0.61 0.810 1.000 2 2010 2014
dbSNP: rs1571878
rs1571878
1 1.000 0.120 6 167127354 intron variant C/T snv 0.61 0.800 1.000 4 2012 2019
dbSNP: rs3093023
rs3093023
7 0.851 0.160 6 167120802 intron variant G/A snv 0.34 0.800 1.000 3 2010 2014
dbSNP: rs1854853
rs1854853
1 1.000 0.120 6 167119574 intron variant A/G snv 0.48 0.800 1.000 1 2014 2014
dbSNP: rs59466457
rs59466457
1 1.000 0.120 6 167124266 intron variant A/G snv 1.6E-03 0.800 1.000 1 2012 2012
dbSNP: rs1556413
rs1556413
1 1.000 0.120 6 167111255 intron variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs1855025
rs1855025
1 1.000 0.120 6 167124106 intron variant A/G snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs2023305
rs2023305
4 0.851 0.280 6 167111410 intron variant C/T snv 0.38 0.700 1.000 1 2010 2010