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: rs104893717
rs104893717
3 0.925 0.040 3 122254227 missense variant T/C snv 0.010 1.000 1 2005 2005
dbSNP: rs200673016
rs200673016
3 0.925 0.040 3 122254221 missense variant T/C snv 4.2E-05 0.010 1.000 1 2005 2005