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: rs1290790
rs1290790
2 3 169373781 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9290366
rs9290366
3 3 169399217 intron variant A/G snv 0.57 0.700 1.000 1 2016 2016