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: rs8000189
rs8000189
10 0.776 0.080 13 110423534 intron variant C/T snv 0.61 0.700 1.000 1 2019 2019