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: rs7096385
rs7096385
1 1.000 0.080 10 67905124 intron variant T/C;G snv 0.700 1.000 1 2018 2018