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: rs39335
rs39335
1 1.000 0.040 7 103813122 intron variant T/C snv 0.21 0.010 1.000 1 2013 2013