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: rs3850195
rs3850195
1 3 171901726 intron variant A/G snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs9832169
rs9832169
1 3 171928252 intron variant G/A snv 0.20 0.700 1.000 1 2018 2018