rs222020, GC

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.851 0.320 4 71770555 intron variant C/T snv 0.72 0.010 1.000 1 2016 2016
Encephalopathies
CUI: C0085584
Disease: Encephalopathies
64 0.851 0.320 4 71770555 intron variant C/T snv 0.72 0.010 1.000 1 2017 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.851 0.320 4 71770555 intron variant C/T snv 0.72 0.010 1.000 1 2017 2017
Peripheral arthritis
CUI: C0238694
Disease: Peripheral arthritis
15 0.851 0.320 4 71770555 intron variant C/T snv 0.72 0.010 1.000 1 2011 2011
Rickets
CUI: C0035579
Disease: Rickets
16 0.851 0.320 4 71770555 intron variant C/T snv 0.72 0.010 1.000 1 2013 2013