ClinVar Miner

List of variants in gene CCDC141 studied for congenital hypogonadotropic hypogonadism

Included ClinVar conditions (68):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_173648.4(CCDC141):c.1667A>G (p.Tyr556Cys) rs141003457 0.01226
NM_173648.4(CCDC141):c.4369G>A (p.Val1457Ile) rs145610810 0.00504
NM_173648.4(CCDC141):c.1521A>C (p.Gln507His) rs114129666 0.00468
NM_173648.4(CCDC141):c.2299G>A (p.Asp767Asn) rs141939661 0.00367
NM_173648.4(CCDC141):c.187C>T (p.Leu63Phe) rs2043530237

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