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: rs174536
rs174536
MYRF ; TMEM258
3 11 61784455 non coding transcript exon variant A/C snv 0.29 0.700 1.000 2 2012 2013