Source: ALL
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: rs7739264
rs7739264
LOC100506885
1 1.000 0.040 6 19785357 intron variant C/G;T snv 0.810 1.000 2 2012 2015