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: rs77150043
rs77150043
14 0.724 0.240 16 50270338 intron variant C/T snv 0.17 0.700 1.000 1 2015 2015