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: rs10206961
rs10206961
2 0.925 0.080 2 85587861 intron variant C/T snv 0.53 0.020 1.000 2 2016 2018