DisGeNET - a database of gene-disease associations

SIFRIM-HITZ-WEISS SYNDROME, C4310688

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:

rs201992075

rs201992075

CHD4 ; SCARNA11

T

0.800

CausalMutation

CLINVAR

dbSNP:

rs201992075

rs201992075

CHD4 ; SCARNA11

0.800

GeneticVariation

UNIPROT

dbSNP:

rs886039915

rs886039915

CHD4

T

0.800

CausalMutation

CLINVAR

dbSNP:

rs886039915

rs886039915

CHD4

0.800

GeneticVariation

UNIPROT

dbSNP:

rs886039916

rs886039916

CHD4

0.800

GeneticVariation

UNIPROT

dbSNP:

rs886039916

rs886039916

CHD4

T

0.800

CausalMutation

CLINVAR

dbSNP:

rs886039917

rs886039917

CHD4

0.800

GeneticVariation

UNIPROT

dbSNP:

rs886039917

rs886039917

CHD4

T

0.800

CausalMutation

CLINVAR

dbSNP:

rs886039918

rs886039918

CHD4

A

0.800

CausalMutation

CLINVAR

dbSNP:

rs886039918

rs886039918

CHD4

0.800

GeneticVariation

UNIPROT

dbSNP:

rs886039919

rs886039919

CHD4

0.800

GeneticVariation

UNIPROT

dbSNP:

rs886039919

rs886039919

CHD4

A

0.800

CausalMutation

CLINVAR

dbSNP:

rs1060499583

rs1060499583

CHD4

C

0.700

GeneticVariation

CLINVAR