DisGeNET - a database of gene-disease associations

Progeria, C0033300

Variant: rs113436208 ×

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:

rs113436208

rs113436208

LMNA

A

0.700

CausalMutation

CLINVAR

Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes.

2007

dbSNP:

rs113436208

rs113436208

LMNA

C

0.700

CausalMutation

CLINVAR