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: rs2930357
rs2930357
1 1.000 0.080 8 3852138 intron variant T/C;G snv 0.010 1.000 1 2014 2014