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: rs16948401
rs16948401
1 17 47810372 intron variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs2074188
rs2074188
1 17 47810885 intron variant C/A;G snv 1.9E-05; 0.53 0.700 1.000 1 2019 2019