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: rs2456181
rs2456181
2 1.000 5 177023836 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs58400555
rs58400555
2 1.000 5 177027080 intron variant A/C;G;T snv 0.700 1.000 1 2018 2018