RS386833851 RECQL4

Health Risk Chr 8:144513126
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Rapadilino syndrome
Baller-Gerold syndrome
Hereditary cancer-predisposing syndrome
Rothmund-Thomson syndrome type 2
Rapadilino syndrome
Baller-Gerold syndrome
Hereditary cancer-predisposing syndrome
Rothmund-Thomson syndrome type 2
Other Variants in RECQL4
rs786200887 rs137853229 rs752729755 rs386833849 rs386833845 rs117642173 rs137853231 rs137853232 rs786200889 rs760363252
Ask Dr. Hemsworth about this variant