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: rs162171
rs162171
1 14 80794033 intron variant A/C snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs17111237
rs17111237
1 14 80939997 intron variant A/G snv 0.15 0.700 1.000 1 2019 2019