RS587777562 PGM3

Health Risk Chr 6:83181786
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What This Variant Does
"CLNSIG=5
Associated Conditions
Immunodeficiency 23
Inborn genetic diseases
Severe combined immunodeficiency disease
Immunodeficiency 23
Inborn genetic diseases
Severe combined immunodeficiency disease
Other Variants in PGM3
rs587777413 rs587777414 rs587777415 rs587777416 rs267608260 rs267608261 rs587777564 rs587777565 rs267608259 rs869312886
Ask Dr. Hemsworth about this variant