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: rs111827672
rs111827672
1 19 37158964 intron variant T/A snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs78241494
rs78241494
1 19 37158846 intron variant T/C snv 0.24 0.700 1.000 1 2019 2019