Source: CLINVAR

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: rs137853197
rs137853197
NEXN
0.925 0.040 1 77942756 missense variant A/G snv 7.2E-05 1.0E-04
CUI: C2751084
Disease: Cardiomyopathy, Dilated, 1CC
Cardiomyopathy, Dilated, 1CC 		0.800 1.000 0 2009 2009
dbSNP: rs137853197
rs137853197
NEXN
0.925 0.040 1 77942756 missense variant A/G snv 7.2E-05 1.0E-04
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		0.700 1.000 1 2009 2009
dbSNP: rs137853197
rs137853197
NEXN
0.925 0.040 1 77942756 missense variant A/G snv 7.2E-05 1.0E-04
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		0.700 0