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: rs16942751
rs16942751
3 1.000 0.080 18 26813249 intron variant C/A;T snv 0.700 1.000 4 2018 2019
dbSNP: rs151246
rs151246
2 18 26869139 intron variant T/G snv 0.77 0.700 1.000 1 2018 2018
dbSNP: rs162005
rs162005
1 18 26867822 intron variant G/A snv 0.78 0.700 1.000 1 2019 2019