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: rs12495941
rs12495941
5 0.851 0.280 3 186850391 intron variant G/T snv 0.35 0.010 1.000 1 2011 2011
dbSNP: rs3774261
rs3774261
10 0.776 0.320 3 186853770 splice region variant A/G snv 0.55 0.010 1.000 1 2011 2011
dbSNP: rs822391
rs822391
4 0.925 0.080 3 186846014 intron variant C/T snv 0.85 0.010 1.000 1 2011 2011
dbSNP: rs822396
rs822396
16 0.732 0.400 3 186849088 intron variant G/A snv 0.81 0.010 1.000 1 2011 2011