DisGeNET - a database of gene-disease associations

MECKEL SYNDROME 12, C4015701

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

N.diseases _v

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF_EXOME

AF_GENOME

Score _vda

EI _vda

N. PMIDs

First Ref.

Last Ref.

dbSNP:

rs786201012

rs786201012

KIF14

1

1.000

1

200603951

frameshift variant

CT/-

delins

7.0E-06

0.700

dbSNP:

rs786201013

rs786201013

KIF14

1

1.000

1

200603922

stop gained

T/A

snv

0.700