DisGeNET - a database of gene-disease associations

rs1251713297, PRMT7

N. diseases: 15

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Obesity

CUI:	C0028754
Disease:	Obesity

0.700

CausalMutation

CLINVAR

Insulin Resistance

CUI:	C0021655
Disease:	Insulin Resistance

0.700

CausalMutation

CLINVAR

Self-Injurious Behavior

CUI:	C0085271
Disease:	Self-Injurious Behavior

0.700

CausalMutation

CLINVAR

Short metacarpal

CUI:	C1837084
Disease:	Short metacarpal

0.700

CausalMutation

CLINVAR

Abnormality of the dentition

CUI:	C0262444
Disease:	Abnormality of the dentition

0.700

CausalMutation

CLINVAR

Serum lipids high (finding)

CUI:	C0428465
Disease:	Serum lipids high (finding)

0.700

CausalMutation

CLINVAR

Dysmorphic facies

CUI:	C0424503
Disease:	Dysmorphic facies

0.700

CausalMutation

CLINVAR

Lumbar hyperlordosis

CUI:	C1184923
Disease:	Lumbar hyperlordosis

0.700

CausalMutation

CLINVAR

Short stature

CUI:	C0349588
Disease:	Short stature

0.700

CausalMutation

CLINVAR

Congenital hypoplasia of kidney

CUI:	C0266295
Disease:	Congenital hypoplasia of kidney

0.700

CausalMutation

CLINVAR

Steatohepatitis

CUI:	C2711227
Disease:	Steatohepatitis

0.700

CausalMutation

CLINVAR

Acanthosis Nigricans

CUI:	C0000889
Disease:	Acanthosis Nigricans

0.700

CausalMutation

CLINVAR

Severe intellectual disability

CUI:	C0036857
Disease:	Severe intellectual disability

0.700

CausalMutation

CLINVAR

Skeletal dysplasia

CUI:	C0410528
Disease:	Skeletal dysplasia

0.700

CausalMutation

CLINVAR

Brachydactyly

CUI:	C0221357
Disease:	Brachydactyly

0.700

CausalMutation

CLINVAR