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HLA-DQB1 and nephrotic syndrome are reported together in 1 article.

HGNC
HGNC:4944
40articles
40mentions
1variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
108articles
108mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

1 records shown · first 60

HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.

PMID 29277510 | PMCID PMC5828864 | DOI 10.1053/j.ajkd.2017.10.013 · American journal of kidney diseases : the official journal of the National Kidney Foundation · 2018 · 9 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneHLA-DQB1“HLA-DQA1*0201, HLA-DQB1*0201, and HLA-DRB1*0701 were the classic HLA alleles with the most significant associations with SSNS risk.”0.98hgnc_dict_v1
phenotypenephrotic syndrome“HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.”0.98phenotype_alias_lexicon_v2
geneHLA-DQA1“HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.”0.98hgnc_dict_v1
geneAPOL1“HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.”0.98hgnc_dict_v1