RS199422311 TINF2

Health Risk Chr 14:24240633
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What This Variant Does
"CLNSIG=5
Associated Conditions
Dyskeratosis congenita
autosomal dominant 1
TINF2-related disorder
Dyskeratosis congenita
autosomal dominant 1
TINF2-related disorder
Other Variants in TINF2
rs121918543 rs121918544 rs121918545 rs387907153 rs1594551449 rs387907154 rs863223324 rs142777869 rs199422315 rs199422314
Ask Dr. Hemsworth about this variant