List of variants in gene combination CHMP2B, POU1F1 reported as benign for congenital hypogonadotropic hypogonadism

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000306.4(POU1F1):c.*140A>T	rs33936108	0.33253
NM_000306.4(POU1F1):c.*139T>A	rs4988463	0.13634
NM_000306.4(POU1F1):c.666-5G>A	rs76296626	0.00674
NM_000306.4(POU1F1):c.*138T>A	rs190287993
NM_000306.4(POU1F1):c.*213=	rs6792500

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