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: rs73057087
rs73057087
1 1.000 0.040 3 33026776 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs6780220
rs6780220
3 0.882 0.120 3 33045708 non coding transcript exon variant A/C snv 0.19 0.010 1.000 1 2016 2016