rs62641228, PEX26

N. diseases: 4
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.
PEROXISOME BIOGENESIS DISORDER 7B
CUI: C3553951
Disease: PEROXISOME BIOGENESIS DISORDER 7B
5 0.882 0.080 22 18079935 missense variant C/G;T snv 7.2E-05 0.800 1.000 6 2003 2017
PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A
CUI: C3539168
Disease: PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A
3 0.882 0.080 22 18079935 missense variant C/G;T snv 7.2E-05 0.700 1.000 6 2003 2017
Peroxisome biogenesis disorders
CUI: C1832200
Disease: Peroxisome biogenesis disorders
38 0.882 0.080 22 18079935 missense variant C/G;T snv 7.2E-05 0.700 1.000 2 2006 2010
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER)
CUI: C3888385
Disease: PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER)
7 0.882 0.080 22 18079935 missense variant C/G;T snv 7.2E-05 0.700 0