RS786203714 PALB2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Basal cell carcinoma
Generalized hypopigmentation
Hereditary breast ovarian cancer syndrome
Familial cancer of breast
Malignant tumor of breast
Hereditary cancer-predisposing syndrome
Hereditary breast ovarian cancer syndrome
Hereditary cancer-predisposing syndrome
Basal cell carcinoma
Generalized hypopigmentation
Hereditary breast ovarian cancer syndrome
Familial cancer of breast
Malignant tumor of breast
Hereditary cancer-predisposing syndrome
Other Variants in PALB2