rs267607117, TMEM67

N. diseases: 2
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.
NEPHRONOPHTHISIS 11
CUI: C3150796
Disease: NEPHRONOPHTHISIS 11
6 0.925 0.080 8 93780747 missense variant G/T snv 0.800 1.000 1 2009 2009
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.925 0.080 8 93780747 missense variant G/T snv 0.010 1.000 1 2009 2009