DisGeNET - a database of gene-disease associations

Source: BEFREE

Disease: Multiple Myeloma ×

Variant: rs974120 ×

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs974120

rs974120

CUI:	C0026764
Disease:	Multiple Myeloma

Multiple Myeloma

0.010

GeneticVariation

BEFREE

In GWAS, rs974120 (8p23.2) reached genomewide significance (P=2.94×10<sup>-9</sup> ), with a nominal significance in MM.

2017