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: rs255052
rs255052
4 0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 0.800 1.000 4 2008 2019
dbSNP: rs56303487
rs56303487
1 16 67995836 intron variant C/T snv 0.22 0.700 1.000 1 2018 2018