RS768642155 JAG1
Upload your DNA to see your genotype for this variant.
Associated Conditions
Isolated Nonsyndromic Congenital Heart Disease
Alagille syndrome due to a JAG1 point mutation
Charcot-Marie-Tooth disease
axonal
Type 2HH
Deafness
congenital heart defects
and posterior embryotoxon
Tetralogy of Fallot
Isolated Nonsyndromic Congenital Heart Disease
Alagille syndrome due to a JAG1 point mutation
Charcot-Marie-Tooth disease
axonal
Type 2HH
Deafness
Other Variants in JAG1