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: rs243865
rs243865
48 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 1.000 2 2011 2018
dbSNP: rs243847
rs243847
1 1.000 0.080 16 55490086 intron variant T/C snv 0.36 0.010 1.000 1 2011 2011