RS387907153 TINF2

Health Risk Chr 14:24240675
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What This Variant Does
"CLNSIG=5
Associated Conditions
Dyskeratosis congenita
autosomal dominant 3
Dyskeratosis congenita
autosomal dominant 3
Other Variants in TINF2
rs121918543 rs121918544 rs121918545 rs1594551449 rs387907154 rs863223324 rs142777869 rs199422311 rs199422315 rs199422314
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