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: rs738409
rs738409
88 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.100 1.000 14 2011 2019
dbSNP: rs2281135
rs2281135
10 0.851 0.160 22 43936690 intron variant G/A snv 0.19 0.010 1.000 1 2019 2019