RS730881972 STK11
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What This Variant Does
"c.487G>
Associated Conditions
Hereditary cancer-predisposing syndrome
Familial pancreatic carcinoma
Melanoma
cutaneous malignant
susceptibility to
1
Germ cell tumor of testis
Peutz-Jeghers syndrome
Hereditary cancer-predisposing syndrome
Familial pancreatic carcinoma
Melanoma
cutaneous malignant
susceptibility to
1
Germ cell tumor of testis
Other Variants in STK11