RS886041782 JAG1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Deafness
congenital heart defects
and posterior embryotoxon
Tetralogy of Fallot
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
Alagille syndrome due to a JAG1 point mutation
Charcot-Marie-Tooth disease
axonal
Other Variants in JAG1