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: rs121912745
rs121912745
9 0.807 0.200 17 44255708 missense variant G/A;T snv 0.700 0
dbSNP: rs121912756
rs121912756
1 17 44257538 missense variant C/T snv 8.0E-06 0.700 0