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: rs10920654
rs10920654
1 1.000 0.080 1 190162620 intron variant C/T snv 0.22 0.700 1.000 1 2019 2019