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: rs2302589
rs2302589
1 1.000 0.040 2 102008324 intron variant C/T snv 0.17 0.010 1.000 1 2015 2015