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: rs1036332
rs1036332
2 1 199043349 intron variant A/C snv 0.70 0.700 1.000 1 2016 2016
dbSNP: rs6427756
rs6427756
1 1 199031598 intron variant A/G snv 0.71 0.700 1.000 1 2018 2018