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: rs1555411378
rs1555411378
2 0.925 0.080 14 102033157 missense variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs387906739
rs387906739
3 0.882 0.200 14 102039416 missense variant A/C snv 0.010 1.000 1 2012 2012
dbSNP: rs387906740
rs387906740
3 0.882 0.200 14 102002546 missense variant G/A snv 0.010 1.000 1 2012 2012