DisGeNET - a database of gene-disease associations

Opitz GBBB Syndrome, X-Linked, C2936904

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:

rs1569268013

rs1569268013

MID1

TC

0.700

CausalMutation

CLINVAR

dbSNP:

rs1569268029

rs1569268029

MID1

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs1569270035

rs1569270035

MID1

T

0.700

CausalMutation

CLINVAR

dbSNP:

rs387906719

rs387906719

MID1

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs398123341

rs398123341

MID1

C

0.700

CausalMutation

CLINVAR

dbSNP:

rs398123342

rs398123342

MID1

TG

0.700

CausalMutation

CLINVAR

dbSNP:

rs745554420

rs745554420

MID1

A

0.700

CausalMutation

CLINVAR