Source: ALL

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: rs397516248
rs397516248
MYH7 ; MHRT
0.851 0.200 14 23415153 missense variant C/T snv
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		0.700 1.000 2 2009 2014
dbSNP: rs1060501439
rs1060501439
MYH7
0.925 0.080 14 23424938 missense variant T/A snv
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		0.700 0
dbSNP: rs587782961
rs587782961
MYH7
1.000 0.040 14 23430936 missense variant T/C snv
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		0.700 0
dbSNP: rs606231324
rs606231324
MYH7
0.851 0.080 14 23428505 missense variant C/G;T snv
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		0.700 0
dbSNP: rs760187215
rs760187215
MYH7
1.000 0.040 14 23431859 missense variant C/T snv 8.0E-06
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		0.700 0