RS121913321 STK11

Health Risk Chr 19:1221314 delins frameshift variant
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What This Variant Does
"c.842delC (p.Pro281Argfs)
Associated Conditions
Peutz-Jeghers syndrome
Hereditary cancer-predisposing syndrome
Melanoma
Familial ovarian cancer
Peutz-Jeghers syndrome
Hereditary cancer-predisposing syndrome
Neoplasm
Peutz-Jeghers syndrome
Peutz-Jeghers syndrome
Hereditary cancer-predisposing syndrome
Melanoma
Familial ovarian cancer
Peutz-Jeghers syndrome
Hereditary cancer-predisposing syndrome
Neoplasm
Population Frequencies
gnomAD ALL
100%
Other Variants in STK11
rs137853075 rs587776656 rs587776657 rs587776658 rs137853076 rs587776659 rs137853077 rs587776660 rs137854584 rs137853078
Ask Dr. Hemsworth about this variant