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: rs10038271
rs10038271
1 1.000 0.040 5 157043390 intron variant C/T snv 0.16 0.700 1.000 1 2011 2011