RS121918351 JAG1

Health Risk Chr 20:10658611
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What This Variant Does
"[OMIM:?]
Associated Conditions
Alagille syndrome due to a JAG1 point mutation
Arteriohepatic dysplasia
Tetralogy of Fallot
Charcot-Marie-Tooth disease
axonal
Type 2HH
Deafness
congenital heart defects
and posterior embryotoxon
Alagille syndrome due to a JAG1 point mutation
Arteriohepatic dysplasia
Tetralogy of Fallot
Charcot-Marie-Tooth disease
axonal
Type 2HH
Other Variants in JAG1
rs1568792286 rs1568791920 rs876660978 rs1568795820 rs121918350 rs886039393 rs28939668 rs121918352 rs121918353 rs397515876
Ask Dr. Hemsworth about this variant