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: rs2531154
rs2531154
1 1.000 0.040 4 16016701 intron variant C/T snv 0.89 0.800 1.000 1 2013 2013