RS398123052 RTEL1

Health Risk Chr 20:63689115
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What This Variant Does
"CLNSIG=5
Associated Conditions
Dyskeratosis congenita
autosomal dominant 4
Dyskeratosis congenita
autosomal dominant 4
Other Variants in RTEL1
rs201540674 rs370343781 rs398123017 rs398123018 rs587777037 rs398123048 rs398123050 rs398123051 rs373740199 rs863223336
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