rs104894204, CSRP3

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.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12
CUI: C2677491
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12
5 0.882 0.040 11 19188245 missense variant A/C snv 0.800 1.000 5 2003 2016
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.882 0.040 11 19188245 missense variant A/C snv 0.030 1.000 3 2004 2018
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.882 0.040 11 19188245 missense variant A/C snv 0.010 1.000 1 2018 2018
Hypertrophic obstructive cardiomyopathy
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
90 0.882 0.040 11 19188245 missense variant A/C snv 0.010 1.000 1 2004 2004