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: rs2003869
rs2003869
2 0.925 0.120 4 108105258 intron variant A/C;G;T snv 0.800 1.000 2 2013 2016
dbSNP: rs898518
rs898518
2 0.925 0.120 4 108095668 intron variant C/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs7690934
rs7690934
2 0.925 0.120 4 108104709 intron variant T/C snv 0.57 0.700 1.000 1 2017 2017