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: rs9364554
rs9364554
3 0.882 0.160 6 160412632 intron variant C/T snv 0.21 0.710 1.000 4 2008 2018
dbSNP: rs3123636
rs3123636
1 1.000 0.080 6 160421505 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs7758229
rs7758229
16 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2015 2015