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
dbSNP: rs2279015
rs2279015
SLC11A1
3 0.882 0.080 2 218394547 non coding transcript exon variant G/A snv 0.51 0.010 1.000 1 2015 2015