List of variants in gene GPR179 reported as benign for not specified

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001004334.4(GPR179):c.909= (p.Val303=)	rs9894059	0.24635
NM_001004334.4(GPR179):c.5605C>G (p.Gln1869Glu)	rs4399578	0.05465
NM_001004334.4(GPR179):c.1478= (p.His493=)	rs4550493	0.04915
NM_001004334.4(GPR179):c.2392G>A (p.Ala798Thr)	rs78470373	0.01044
NM_001004334.4(GPR179):c.3454T>C (p.Ser1152Pro)	rs149252987	0.00689
NM_001004334.4(GPR179):c.6336G>A (p.Ala2112=)	rs186214845	0.00296
NM_001004334.4(GPR179):c.4306C>T (p.Arg1436Trp)	rs147966258	0.00228
NM_001004334.4(GPR179):c.5019C>G (p.Thr1673=)	rs182907807	0.00219
NM_001004334.4(GPR179):c.5975G>A (p.Gly1992Asp)	rs200936863	0.00160
NM_001004334.4(GPR179):c.6824T>C (p.Leu2275Pro)	rs148601715	0.00108
NM_001004334.4(GPR179):c.3441C>T (p.Ser1147=)	rs377711366	0.00054
NM_001004334.4(GPR179):c.2022C>T (p.Asp674=)	rs79623844	0.00041
NM_001004334.4(GPR179):c.795-4G>A	rs150772690	0.00038
NM_001004334.4(GPR179):c.1839C>T (p.Phe613=)	rs746417155	0.00008

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