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Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

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MSH2 and infertility are reported together in 1 article.

Gene

MSH2

HGNC
HGNC:7325
24articles
24mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype

Infertility

199articles
199mentions
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
TypeEntitySource evidenceConfidenceExtractor
geneMSH2“Association between promoter methylation of MLH1 and MSH2 and reactive oxygen species in oligozoospermic men-A pilot study.”0.98hgnc_dict_v1
phenotypeinfertility“MLH1 and MSH2 are important genes for DNA mismatch repair and crossing over during meiosis and are implicated in male infertility.”0.98phenotype_alias_lexicon_v2
geneMLH1“Association between promoter methylation of MLH1 and MSH2 and reactive oxygen species in oligozoospermic men-A pilot study.”0.98hgnc_dict_v1