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: rs7184253
rs7184253
1 16 67346647 intron variant T/C snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs8055190
rs8055190
2 16 67357715 intron variant C/G;T snv 0.700 1.000 1 2017 2017