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FSHR and recurrent pregnancy loss are reported together in 1 article.

Gene

FSHR

HGNC
HGNC:3969
10articles
10mentions
2variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
36articles
36mentions
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

A genomics approach to females with infertility and recurrent pregnancy loss.

PMID 32172300 | DOI 10.1007/s00439-020-02143-5 · Human genetics · 2020 · 17 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneFSHR“These include variants in previously established female infertility-related genes (TLE6, NLRP7, FSHR, and ZP1) as well as genes with only tentative links in the literature (NLRP5).”0.98hgnc_dict_v1
phenotyperecurrent pregnancy loss“A genomics approach to females with infertility and recurrent pregnancy loss.”0.98phenotype_alias_lexicon_v2
geneTLE6“These include variants in previously established female infertility-related genes (TLE6, NLRP7, FSHR, and ZP1) as well as genes with only tentative links in the literature (NLRP5).”0.98hgnc_dict_v1
geneNLRP7“These include variants in previously established female infertility-related genes (TLE6, NLRP7, FSHR, and ZP1) as well as genes with only tentative links in the literature (NLRP5).”0.98hgnc_dict_v1