Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4746172
rs4746172
VCL
10 74096084 intron variant C/T snv 0.73
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.010 1.000 1 2015 2015
dbSNP: rs4746172
rs4746172
VCL
10 74096084 intron variant C/T snv 0.73
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2015 2015
dbSNP: rs4746172
rs4746172
VCL
10 74096084 intron variant C/T snv 0.73
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2015 2015