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: rs7934606
rs7934606
2 1.000 0.040 11 1100037 intron variant C/G;T snv 0.810 1.000 2 2013 2016