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: rs2798224
rs2798224
2 1.000 0.120 4 3265941 intron variant G/A snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs3095073
rs3095073
1 1.000 0.120 4 3261411 missense variant G/A snv 0.33 0.33 0.700 1.000 1 2012 2012
dbSNP: rs3095079
rs3095079
1 1.000 0.120 4 3263687 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3129319
rs3129319
1 1.000 0.120 4 3263654 intron variant A/G snv 0.37 0.700 1.000 1 2012 2012