Gene: SLC10A2 ×
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: rs188096
rs188096
SLC10A2
1 1.000 0.080 13 103052694 missense variant A/C snv 0.85 0.89 0.010 1.000 1 2008 2008
dbSNP: rs41281678
rs41281678
SLC10A2
1 1.000 0.080 13 103052700 synonymous variant G/A snv 1.9E-02 2.7E-02 0.010 1.000 1 2008 2008