RS386833845 RECQL4

Health Risk Chr 8:144514983
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rothmund-Thomson syndrome
Rapadilino syndrome
Baller-Gerold syndrome
B lymphoblastic leukemia lymphoma with t(12
21)(p13
q22)
TEL-AML1 (ETV6-RUNX1)
High grade surface osteosarcoma
Rothmund-Thomson syndrome type 2
Inborn genetic diseases
RECQL4-related disorder
Rothmund-Thomson syndrome
Rapadilino syndrome
Baller-Gerold syndrome
B lymphoblastic leukemia lymphoma with t(12
Other Variants in RECQL4
rs786200887 rs137853229 rs752729755 rs386833849 rs117642173 rs137853231 rs137853232 rs786200889 rs760363252 rs386833843
Ask Dr. Hemsworth about this variant