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: rs7517357
rs7517357
1 1.000 0.040 1 7965215 intron variant C/T snv 0.14 0.010 1.000 1 2012 2012