RS1555247936 MED13L

Health Risk Chr 12:116008723
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Associated Conditions
Inborn genetic diseases
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
Inborn genetic diseases
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
Other Variants in MED13L
rs869025286 rs869025287 rs869025288 rs869025289 rs147976828 rs869025291 rs869312875 rs869312707 rs879255407 rs886039599
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