RS918046091 JAG1

Health Risk Chr 20:10639631
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Associated Conditions
Alagille syndrome due to a JAG1 point mutation
Cardiovascular phenotype
JAG1-related disorder
Deafness
congenital heart defects
and posterior embryotoxon
Tetralogy of Fallot
Charcot-Marie-Tooth disease
axonal
Type 2HH
Alagille syndrome due to a JAG1 point mutation
Cardiovascular phenotype
JAG1-related disorder
Deafness
congenital heart defects
Other Variants in JAG1
rs1568792286 rs1568791920 rs876660978 rs1568795820 rs121918350 rs121918351 rs886039393 rs28939668 rs121918352 rs121918353
Ask Dr. Hemsworth about this variant