Gene: SLC22A11 ×
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: rs147522958
rs147522958
SLC22A11
1 1.000 0.080 11 64564318 missense variant G/A snv 4.9E-04 3.1E-04 0.010 1.000 1 2008 2008
dbSNP: rs72559737
rs72559737
SLC22A11
1 1.000 0.080 11 64559224 synonymous variant C/A;G snv 1.3E-02 0.010 1.000 1 2008 2008