RS137853229 RECQL4
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What This Variant Does
"[OMIM:?]
Associated Conditions
Rothmund-Thomson syndrome
Baller-Gerold syndrome
Inborn genetic diseases
Rapadilino syndrome
Rothmund-Thomson syndrome type 2
Hereditary cancer-predisposing syndrome
RECQL4-related disorder
Rothmund-Thomson syndrome
Baller-Gerold syndrome
Inborn genetic diseases
Rapadilino syndrome
Rothmund-Thomson syndrome type 2
Hereditary cancer-predisposing syndrome
RECQL4-related disorder
Other Variants in RECQL4