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: rs76622665
rs76622665
1 5 65395057 intron variant T/C snv 9.3E-03 0.700 1.000 1 2019 2019
dbSNP: rs79303598
rs79303598
1 5 65249673 intron variant C/A;T snv 0.700 1.000 1 2019 2019