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: rs731779
rs731779
1 1.000 0.040 13 46877903 intron variant A/C snv 0.16 0.010 1.000 1 2010 2010