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: rs7010162
rs7010162
2 1.000 0.120 8 70064270 intron variant C/T snv 0.52 0.800 1.000 3 2013 2017