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: rs11155372
rs11155372
3 0.925 0.040 6 144698602 intron variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs9321987
rs9321987
3 0.925 0.040 6 144709148 intron variant C/T snv 0.40 0.700 1.000 1 2018 2018