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: rs10927875
rs10927875
3 1.000 0.040 1 15972817 intron variant C/T snv 0.29 0.800 1.000 1 2011 2011