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: rs174528
rs174528
MYRF ; TMEM258
5 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 2 2012 2013