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: rs121907896
rs121907896
SLC22A12
5 0.851 0.200 11 64591825 missense variant G/A snv 1.8E-04 8.4E-05 0.010 1.000 1 2007 2007