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: rs145641996
rs145641996
1.000 0.040 1 11792285 missense variant T/C;G snv 1.6E-05; 1.6E-04
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.010 1.000 1 2015 2015
dbSNP: rs145641996
rs145641996
1.000 0.040 1 11792285 missense variant T/C;G snv 1.6E-05; 1.6E-04
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2015 2015