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: rs4132748
rs4132748
2 3 67405379 intron variant T/C snv 0.73 0.700 1.000 2 2019 2019
dbSNP: rs1490265
rs1490265
2 1.000 0.040 3 67401619 intron variant C/A snv 0.74 0.700 1.000 1 2017 2017