EN2, engrailed homeobox 2, 2020

N. diseases: 41; N. variants: 8
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: rs1345514
rs1345514
1.000 0.040 7 155456455 intron variant C/T snv 0.29
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease
Nervous System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs3808330
rs3808330
1.000 0.040 7 155463312 3 prime UTR variant T/C snv 0.23
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease
Nervous System Diseases 0.010 1.000 1 2009 2009