RS750855317 JAG1

Health Risk Chr 20:10646989
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Associated Conditions
Alagille syndrome due to a JAG1 point mutation
Cardiovascular phenotype
Tetralogy of Fallot
Deafness
congenital heart defects
and posterior embryotoxon
Charcot-Marie-Tooth disease
axonal
Type 2HH
JAG1-related disorder
Alagille syndrome due to a JAG1 point mutation
Cardiovascular phenotype
Tetralogy of Fallot
Deafness
congenital heart defects
Other Variants in JAG1
rs1568792286 rs1568791920 rs876660978 rs1568795820 rs121918350 rs121918351 rs886039393 rs28939668 rs121918352 rs121918353
Ask Dr. Hemsworth about this variant