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: rs3807307
rs3807307
6 0.827 0.120 7 128939148 intron variant T/C snv 0.41 0.800 1.000 1 2012 2012
dbSNP: rs3757387
rs3757387
6 0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs3778753
rs3778753
2 0.925 0.200 7 128939988 intron variant A/G snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs3778754
rs3778754
1 1.000 0.080 7 128935498 upstream gene variant C/G snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs3807306
rs3807306
8 0.776 0.320 7 128940626 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3823536
rs3823536
2 0.925 0.280 7 128939612 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012