Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039763
rs886039763
HNRNPH2 ; RPL36A-HNRNPH2
T 0.700 GeneticVariation CLINVAR Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females. 27545675

2016
dbSNP: rs886039763
rs886039763
HNRNPH2 ; RPL36A-HNRNPH2
T 0.700 GeneticVariation CLINVAR UniProt: a hub for protein information. 25348405

2015
dbSNP: rs886039763
rs886039763
HNRNPH2 ; RPL36A-HNRNPH2
T 0.700 GeneticVariation CLINVAR De novo mutations in moderate or severe intellectual disability. 25356899

2014