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: rs56396408
rs56396408
1 4 1014598 intron variant C/T snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs76051363
rs76051363
1 4 1013199 intron variant C/G;T snv 0.700 1.000 1 2018 2018