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: rs1160985
rs1160985
6 1.000 0.080 19 44900155 intron variant C/T snv 0.52 0.700 1.000 1 2013 2013