Gene: SLC18A2 ×
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: rs767337086
rs767337086
SLC18A2
1 1.000 0.040 10 117255286 missense variant C/A;G;T snv 2.4E-05; 4.0E-06; 8.0E-06 0.010 1.000 1 2016 2016