List of variants in gene GPR179 reported as uncertain significance by Blueprint Genetics

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_001004334.4(GPR179):c.4703G>A (p.Arg1568Lys)	rs192420703	0.00021
NM_001004334.4(GPR179):c.4052A>C (p.Asp1351Ala)	rs758036832	0.00001
NM_001004334.4(GPR179):c.1154T>G (p.Leu385Arg)	rs2037410656
NM_001004334.4(GPR179):c.5575G>A (p.Val1859Ile)	rs371603020

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