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: rs475688
rs475688
SLC22A12
3 0.882 0.160 11 64596819 intron variant C/T snv 0.25 0.700 1.000 2 2010 2013