rs1555738475, STK11

N. diseases: 12
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Abdominal Pain
CUI: C0000737
Disease: Abdominal Pain
18 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Abnormal pigmentation of the oral mucosa
CUI: C4020959
Disease: Abnormal pigmentation of the oral mucosa
1 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Hamartomatous polyposis
CUI: C3272802
Disease: Hamartomatous polyposis
3 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Intestinal Polyposis
CUI: C1257915
Disease: Intestinal Polyposis
3 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Intussusception
CUI: C0021933
Disease: Intussusception
1 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Iron deficiency anemia
CUI: C0162316
Disease: Iron deficiency anemia
21 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Kidney Neoplasm
CUI: C0022665
Disease: Kidney Neoplasm
11 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Lip hyperpigmentation
CUI: C4021963
Disease: Lip hyperpigmentation
1 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Nausea and vomiting
CUI: C0027498
Disease: Nausea and vomiting
11 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Ovarian Cysts
CUI: C0029927
Disease: Ovarian Cysts
3 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Peutz-Jeghers Syndrome
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
79 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0
Uterine Neoplasms
CUI: C0042138
Disease: Uterine Neoplasms
1 0.776 0.400 19 1220707 frameshift variant G/- delins 0.700 0