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: rs1800932
rs1800932
3 2 47790942 synonymous variant A/G snv 0.13 0.15 0.700 1.000 1 2015 2015
dbSNP: rs76928871
rs76928871
1 2 47778682 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019