List of variants in gene GPR179 reported as likely pathogenic

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001004334.4(GPR179):c.4699_4700del (p.Ser1567fs)	rs369324783	0.00021
NM_001004334.4(GPR179):c.4550dup (p.Met1517fs)	rs756928373	0.00003
NM_001004334.4(GPR179):c.349G>A (p.Asp117Asn)	rs776996552	0.00002
NM_001004334.4(GPR179):c.1429C>T (p.Arg477Ter)	rs764877172	0.00001
NM_001004334.4(GPR179):c.148C>T (p.Gln50Ter)	rs767430727	0.00001
NM_001004334.4(GPR179):c.1573C>T (p.Arg525Ter)	rs773022324	0.00001
NM_001004334.4(GPR179):c.991+1G>T	rs761533717	0.00001
NM_001004334.4(GPR179):c.1296+1G>A	rs779656144
NM_001004334.4(GPR179):c.1645+1G>T
NM_001004334.4(GPR179):c.1646-1G>C
NM_001004334.4(GPR179):c.1727del (p.Tyr576fs)	rs1567725425
NM_001004334.4(GPR179):c.1818G>A (p.Trp606Ter)	rs1268507778
NM_001004334.4(GPR179):c.2427dup (p.Pro810fs)	rs757246221
NM_001004334.4(GPR179):c.2706_2707dup (p.Pro903fs)	rs1200683561
NM_001004334.4(GPR179):c.3138_3139del (p.Glu1046fs)	rs776189685
NM_001004334.4(GPR179):c.4123_4127del (p.Ile1375fs)	rs1741916135
NM_001004334.4(GPR179):c.799_803delinsTGATCTAC (p.Gln267_Val268delinsTer)	rs886043488

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