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: rs104894346
rs104894346
1 1.000 0.200 12 49094511 start lost A/G snv 0.700 0
dbSNP: rs1565573892
rs1565573892
1 1.000 0.200 12 49091322 missense variant C/T snv 0.700 0