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: rs16879765
rs16879765
2 0.925 0.120 7 37949493 intron variant C/T snv 0.13 0.700 1.000 2 2011 2017
dbSNP: rs2598107
rs2598107
2 1.000 0.120 7 37933412 intron variant C/T snv 0.34 0.700 1.000 1 2017 2017