FLCN, folliculin, 201163

N. diseases: 160; N. variants: 127
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060502367
rs1060502367
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1060502369
rs1060502369
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1060502370
rs1060502370
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
C 0.700 CausalMutation CLINVAR
dbSNP: rs1060502371
rs1060502371
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
G 0.700 CausalMutation CLINVAR
dbSNP: rs1064792959
rs1064792959
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CTGAT 0.700 CausalMutation CLINVAR
dbSNP: rs1064792959
rs1064792959
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
CTGAT 0.700 CausalMutation CLINVAR
dbSNP: rs1131690824
rs1131690824
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 CausalMutation CLINVAR
dbSNP: rs1131690825
rs1131690825
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 CausalMutation CLINVAR
dbSNP: rs1131690827
rs1131690827
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1131690828
rs1131690828
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1131690829
rs1131690829
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
AAC 0.700 CausalMutation CLINVAR
dbSNP: rs1131690831
rs1131690831
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
ACGTGC 0.700 CausalMutation CLINVAR
dbSNP: rs1131690836
rs1131690836
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1131690837
rs1131690837
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
TA 0.700 CausalMutation CLINVAR
dbSNP: rs1131690837
rs1131690837
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
TA 0.700 CausalMutation CLINVAR
dbSNP: rs1131690839
rs1131690839
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
GC 0.700 CausalMutation CLINVAR
dbSNP: rs1131690841
rs1131690841
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1135401752
rs1135401752
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
T 0.700 CausalMutation CLINVAR
dbSNP: rs1254608489
rs1254608489
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
A 0.700 CausalMutation CLINVAR
dbSNP: rs1266098984
rs1266098984
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
A 0.700 CausalMutation CLINVAR
dbSNP: rs137852929
rs137852929
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
T 0.700 CausalMutation CLINVAR
dbSNP: rs137852930
rs137852930
Entrez Id: 201163
Gene Symbol: FLCN
FLCN
CUI: C0009402
Disease:
Colorectal Carcinoma
C 0.700 CausalMutation CLINVAR
dbSNP: rs1555607179
rs1555607179
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555607212
rs1555607212
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0346010
Disease:
Multiple fibrofolliculomas
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555607640
rs1555607640
Entrez Id: 23164;201163
Gene Symbol: MPRIP;FLCN
MPRIP;FLCN
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CGT 0.700 CausalMutation CLINVAR