List of variants in gene TH reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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_000360.4(TH):c.1143G>T (p.Gln381His)	rs1846071715
NM_000360.4(TH):c.1162T>C (p.Tyr388His)	rs1846070989
NM_000360.4(TH):c.1378G>T (p.Asp460Tyr)	rs374629948
NM_000360.4(TH):c.920T>C (p.Val307Ala)	rs2495803118

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