HMOX2, heme oxygenase 2, 3163

N. diseases: 31; N. variants: 4
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: rs1051308
rs1051308 		0.882 0.080 16 4510300 3 prime UTR variant G/A snv 0.54
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2270363
rs2270363 		0.882 0.080 16 4476291 5 prime UTR variant A/G snv 0.74
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2011 2011