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: rs7412746
rs7412746
1 1.000 0.040 1 150887995 intron variant C/T snv 0.41 0.800 1.000 2 2011 2017