List of variants in gene HRH4 reported as likely benign

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_021624.4(HRH4):c.227C>T (p.Thr76Met)	rs146877850	0.00007
NM_021624.4(HRH4):c.652G>T (p.Ala218Ser)	rs1910159081	0.00001
NM_021624.4(HRH4):c.1123A>G (p.Ile375Val)
NM_021624.4(HRH4):c.796A>C (p.Lys266Gln)

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