List of variants in gene TGM1 reported as benign by Illumina Laboratory Services, Illumina

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000359.3(TGM1):c.726G>A (p.Glu242=)	rs35755034	0.04892
NM_000359.3(TGM1):c.366G>A (p.Ser122=)	rs17102410	0.03062
NM_000359.3(TGM1):c.54G>A (p.Gln18=)	rs41295336	0.00761
NM_000359.3(TGM1):c.2264C>T (p.Ser755Leu)	rs35926651	0.00599
NM_000359.3(TGM1):c.1819C>T (p.Arg607Cys)	rs2229464	0.00382
NM_000359.3(TGM1):c.383A>G (p.Glu128Gly)	rs138592626	0.00046
NM_000359.3(TGM1):c.1146C>A (p.Gly382=)	rs1126432

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