rs760185784, DSC2

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.
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 18 31089533 missense variant T/C snv 4.0E-06 0.010 1.000 1 2015 2015
Skin Abnormalities
CUI: C0037268
Disease: Skin Abnormalities
16 18 31089533 missense variant T/C snv 4.0E-06 0.010 1.000 1 2015 2015