rs104894205, CSRP3

N. diseases: 3
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 19188286 missense variant A/G snv 1.2E-05 5.6E-05 0.800 1.000 8 2003 2017
CARDIOMYOPATHY, DILATED, 1M
CUI: C1843808
Disease: CARDIOMYOPATHY, DILATED, 1M
4 0.882 0.040 11 19188286 missense variant A/G snv 1.2E-05 5.6E-05 0.700 1.000 4 2006 2017
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.882 0.040 11 19188286 missense variant A/G snv 1.2E-05 5.6E-05 0.010 1.000 1 2018 2018