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: rs2351299
rs2351299
2 1.000 0.040 4 47141348 intron variant G/T snv 0.19 0.010 < 0.001 1 2006 2006