S100B, S100 calcium binding protein B, 6285

N. diseases: 599; N. variants: 6
Disease: Parkinson Disease ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1051169
rs1051169 		0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9722
rs9722 		0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2018 2018