DisGeNET - a database of gene-disease associations

Basal cell carcinoma, C0007117

Variant: rs401681 ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs401681

CLPTM1L

0.700

GeneticVariation

GWASCAT

New basal cell carcinoma susceptibility loci.

25855136

2015

dbSNP:

rs401681

CLPTM1L

0.700

GeneticVariation

GWASCAT

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.

24403052

2014

dbSNP:

rs401681

CLPTM1L

0.700

GeneticVariation

GWASCAT

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.

19151717

2009