List of variants in gene TACR3 reported as uncertain significance by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001059.3(TACR3):c.1321C>T (p.Arg441Cys)	rs146482011	0.00024
NM_001059.3(TACR3):c.918G>A (p.Met306Ile)	rs201088165	0.00005
NM_001059.3(TACR3):c.1289C>T (p.Thr430Met)	rs200736098	0.00001
NM_001059.3(TACR3):c.445A>G (p.Ser149Gly)	rs750591352	0.00001
NM_001059.3(TACR3):c.514A>G (p.Ser172Gly)	rs199505146	0.00001
NM_001059.3(TACR3):c.1345G>T (p.Ala449Ser)	rs17033889
NM_001059.3(TACR3):c.231G>C (p.Gln77His)
NM_001059.3(TACR3):c.250C>A (p.Arg84Ser)	rs1208727441
NM_001059.3(TACR3):c.416C>T (p.Thr139Met)	rs1723155703
NM_001059.3(TACR3):c.686G>C (p.Gly229Ala)
NM_001059.3(TACR3):c.775C>T (p.Pro259Ser)	rs1057524840
NM_001059.3(TACR3):c.892G>T (p.Val298Phe)	rs376656496
NM_001059.3(TACR3):c.916A>G (p.Met306Val)

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