RS886040988 CHD7

Health Risk Chr 8:60830422
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What This Variant Does
"CLNSIG=4
Associated Conditions
CHARGE syndrome
Inborn genetic diseases
CHARGE syndrome
Inborn genetic diseases
Other Variants in CHD7
rs121434338 rs121434339 rs121434340 rs121434341 rs121434342 rs786200873 rs121434343 rs121434344 rs387906271 rs202143667
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