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: rs137853077
rs137853077
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
C 0.810 CausalMutation CLINVAR
dbSNP: rs121913315
rs121913315
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0025202
Disease:
melanoma
T 0.800 CausalMutation CLINVAR
dbSNP: rs121913315
rs121913315
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0025202
Disease:
melanoma
0.800 GeneticVariation UNIPROT
dbSNP: rs137853080
rs137853080
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0025202
Disease:
melanoma
0.800 GeneticVariation UNIPROT
dbSNP: rs137853080
rs137853080
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0025202
Disease:
melanoma
G 0.800 CausalMutation CLINVAR
dbSNP: rs137853081
rs137853081
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0025202
Disease:
melanoma
C 0.800 CausalMutation CLINVAR
dbSNP: rs137853081
rs137853081
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0025202
Disease:
melanoma
0.800 GeneticVariation UNIPROT
dbSNP: rs137853082
rs137853082
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs137853083
rs137853083
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
G 0.710 CausalMutation CLINVAR
dbSNP: rs587776661
rs587776661
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
A 0.710 CausalMutation CLINVAR
dbSNP: rs1057517830
rs1057517830
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1057518830
rs1057518830
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C1257915
Disease:
Intestinal Polyposis
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518830
rs1057518830
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C1844606
Disease:
Periorbital hyperpigmentation
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057520038
rs1057520038
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0009402
Disease:
Colorectal Carcinoma
0.700 GeneticVariation UNIPROT
dbSNP: rs1060499958
rs1060499958
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
C 0.700 CausalMutation CLINVAR
dbSNP: rs1060499960
rs1060499960
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs1060499961
rs1060499961
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs1131690917
rs1131690917
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1131690920
rs1131690920
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1131690920
rs1131690920
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1131690921
rs1131690921
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1131690922
rs1131690922
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
GTACC 0.700 CausalMutation CLINVAR
dbSNP: rs1131690923
rs1131690923
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1131690924
rs1131690924
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 CausalMutation CLINVAR
dbSNP: rs1131690925
rs1131690925
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR