RS879255271 TCF3

Health Risk Chr 19:1612357
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What This Variant Does
"CLNSIG=5
Associated Conditions
Agammaglobulinemia 8
autosomal dominant
Inborn genetic diseases
Agammaglobulinemia 8
autosomal dominant
Inborn genetic diseases
Other Variants in TCF3
rs1555712474 rs138005323 rs7252811 rs201841190 rs1599413207 rs747579840 rs2061880735 rs2074888 rs372696633 rs139492270
Ask Dr. Hemsworth about this variant