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: rs4547811
rs4547811
1 4 145873469 intron variant T/C snv 0.20 0.800 1.000 1 2011 2011
dbSNP: rs4835265
rs4835265
6 4 145900258 intron variant C/A snv 0.15 0.700 1.000 2 2011 2018
dbSNP: rs35146602
rs35146602
1 4 145866089 intron variant A/G snv 0.15 0.700 1.000 1 2019 2019