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: rs6743376
rs6743376
2 2 113074756 missense variant C/A snv 0.69 0.69 0.700 1.000 1 2014 2014
dbSNP: rs6761276
rs6761276
2 2 113074735 missense variant T/C snv 0.56 0.57 0.700 1.000 1 2014 2014