DisGeNET - a database of gene-disease associations

Subclinical hypothyroidism, C0271790

Variant: rs61730030 ×

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:

rs61730030

rs61730030

DUOX2

0.010

GeneticVariation

BEFREE

One child with SH showed H678R, R701Q, and P982A substitutions, and another child with SH showed only the P982A.

2011