DisGeNET - a database of gene-disease associations

Secondary Caesarian section, C4072904

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:

rs1247665387

rs1247665387

FA2H

A

0.700

GeneticVariation

CLINVAR

dbSNP:

rs1294950721

rs1294950721

JAG1

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs1400419650

rs1400419650

TRIP11

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs1421405659

rs1421405659

MYBPC1

C

0.700

GeneticVariation

CLINVAR

dbSNP:

rs142239530

rs142239530

STIM1

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs1555386022

rs1555386022

TRIP11

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs1555462347

rs1555462347

USP7

G

0.700

GeneticVariation

CLINVAR

dbSNP:

rs1555731819

rs1555731819

KMT2B

T

0.700

GeneticVariation

CLINVAR

dbSNP:

rs1560755661

rs1560755661

TBCK

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs1561273261

rs1561273261

KIF2A ; DIMT1

A

0.700

GeneticVariation

CLINVAR

dbSNP:

rs1564421528

rs1564421528

WAC

T

0.700

CausalMutation

CLINVAR

dbSNP:

rs200661329

rs200661329

PIGQ

A

0.700

GeneticVariation

CLINVAR

dbSNP:

rs879255280

rs879255280

SMO

T

0.700

CausalMutation

CLINVAR