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: rs1127787
rs1127787
1 1.000 0.080 12 27714794 missense variant G/A snv 0.14 0.12 0.700 1.000 1 2018 2018
dbSNP: rs7316898
rs7316898
1 1.000 0.080 12 27751631 intron variant T/C;G snv 0.700 1.000 1 2014 2014