List of variants in gene HYOU1 reported as benign for not provided

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_006389.5(HYOU1):c.1726+36A>G	rs673768	0.86764
NM_006389.5(HYOU1):c.2235A>G (p.Ala745=)	rs568922	0.77515
NM_006389.5(HYOU1):c.543C>T (p.Asn181=)	rs538478	0.38158
NM_006389.5(HYOU1):c.1476C>T (p.Asn492=)	rs1804690	0.09125
NM_006389.5(HYOU1):c.363G>A (p.Pro121=)	rs11822958	0.04571
NM_006389.5(HYOU1):c.2511-7C>T	rs7931970	0.04370
NM_006389.5(HYOU1):c.2377-13G>A	rs116733985	0.01882
NM_006389.5(HYOU1):c.510G>A (p.Lys170=)	rs35408224	0.01611
NM_006389.5(HYOU1):c.792A>T (p.Val264=)	rs34446044	0.01507
NM_006389.5(HYOU1):c.794+20G>T	rs77350634	0.00433
NM_006389.5(HYOU1):c.2031C>T (p.Val677=)	rs45450894	0.00389
NM_006389.5(HYOU1):c.2888-13C>G	rs115207968	0.00350
NM_006389.5(HYOU1):c.2355G>A (p.Glu785=)	rs149598298	0.00312
NM_006389.5(HYOU1):c.2487C>G (p.Leu829=)	rs138286788	0.00135
NM_006389.5(HYOU1):c.2029G>A (p.Val677Ile)	rs147081612	0.00126
NM_006389.5(HYOU1):c.294T>G (p.Arg98=)	rs142573589	0.00083
NM_006389.5(HYOU1):c.2888-14T>C	rs189673760	0.00048
NM_006389.5(HYOU1):c.2510+10C>T	rs2298481	0.00036
NM_006389.5(HYOU1):c.1675G>A (p.Val559Ile)	rs116878385	0.00035
NM_006389.5(HYOU1):c.909G>A (p.Pro303=)	rs201944514	0.00026
NM_006389.5(HYOU1):c.420-11C>T	rs549303555	0.00001
NM_006389.5(HYOU1):c.1526+16G>T	rs372920381
NM_006389.5(HYOU1):c.1722C>G (p.Leu574=)
NM_006389.5(HYOU1):c.2254-8dup
NM_006389.5(HYOU1):c.288G>C (p.Thr96=)	rs145661123
NM_006389.5(HYOU1):c.381C>T (p.Phe127=)	rs511134
NM_006389.5(HYOU1):c.419+8C>T

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