STK11, serine/threonine kinase 11, 6794

N. diseases: 372; N. variants: 145
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131690926
rs1131690926
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1131690929
rs1131690929
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
GA 0.700 CausalMutation CLINVAR
dbSNP: rs1131690930
rs1131690930
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
TC 0.700 CausalMutation CLINVAR
dbSNP: rs1131690933
rs1131690933
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
AGAAGC 0.700 CausalMutation CLINVAR
dbSNP: rs1131690936
rs1131690936
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1131690939
rs1131690939
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CG 0.700 CausalMutation CLINVAR
dbSNP: rs1131690941
rs1131690941
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1131690944
rs1131690944
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1131690945
rs1131690945
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1131690946
rs1131690946
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
AC 0.700 CausalMutation CLINVAR
dbSNP: rs1131690948
rs1131690948
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 CausalMutation CLINVAR
dbSNP: rs1131690949
rs1131690949
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CG 0.700 CausalMutation CLINVAR
dbSNP: rs1131690949
rs1131690949
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
CG 0.700 CausalMutation CLINVAR
dbSNP: rs1131690950
rs1131690950
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs1131690952
rs1131690952
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
GA 0.700 CausalMutation CLINVAR
dbSNP: rs1131690953
rs1131690953
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 GeneticVariation CLINVAR
dbSNP: rs121913316
rs121913316
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.700 GeneticVariation UNIPROT
dbSNP: rs121913317
rs121913317
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0009402
Disease:
Colorectal Carcinoma
0.700 GeneticVariation UNIPROT
dbSNP: rs121913322
rs121913322
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C4721610
Disease:
Carcinoma, Ovarian Epithelial
0.700 GeneticVariation UNIPROT
dbSNP: rs121913322
rs121913322
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0029925
Disease:
Ovarian Carcinoma
0.700 GeneticVariation UNIPROT
dbSNP: rs121913322
rs121913322
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C1140680
Disease:
Malignant neoplasm of ovary
0.700 GeneticVariation UNIPROT
dbSNP: rs121913323
rs121913323
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0025202
Disease:
melanoma
T 0.700 CausalMutation CLINVAR
dbSNP: rs121913324
rs121913324
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
T 0.700 CausalMutation CLINVAR
dbSNP: rs137853075
rs137853075
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs137853078
rs137853078
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR