Gene: S100B ×
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: rs2300403
rs2300403
S100B
1 1.000 0.080 21 46601141 intron variant C/A;G;T snv 0.010 1.000 1 2007 2007