rs26907, RASGRF2

N. diseases: 3
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.
Adrenoleukodystrophy
CUI: C0162309
Disease: Adrenoleukodystrophy
116 0.882 0.240 5 81069496 intron variant G/A;T snv 0.010 1.000 1 2016 2016
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.882 0.240 5 81069496 intron variant G/A;T snv 0.010 1.000 1 2016 2016
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.882 0.240 5 81069496 intron variant G/A;T snv 0.010 1.000 1 2016 2016