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: rs481931
rs481931
3 0.882 0.120 1 94104460 intron variant G/T snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs66515264
rs66515264
3 0.882 0.120 1 94092554 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs560426
rs560426
5 0.851 0.200 1 94087882 intron variant C/T snv 0.53 0.010 < 0.001 1 2010 2010