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: rs2276631
rs2276631
SLC11A1
3 0.882 0.120 2 218384290 missense variant C/T snv 0.23 0.23 0.010 1.000 1 2015 2015