rs104894344, FGF23

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.
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2
CUI: C4693863
Disease: TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2
4 0.925 0.120 12 4370713 missense variant G/A snv 0.800 1.000 4 2005 2014
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL
CUI: C1876187
Disease: TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL
3 0.925 0.120 12 4370713 missense variant G/A snv 0.020 1.000 2 2016 2016