List of variants in gene combination LOC121853040, TCN2 reported as uncertain significance for anemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_000355.4(TCN2):c.64+11C>T	rs141519384	0.00203
NM_000355.4(TCN2):c.-98T>G	rs370882214	0.00150
NM_000355.4(TCN2):c.-34A>G	rs199511962	0.00005
NM_000355.3(TCN2):c.-191G>A	rs886057394	0.00004
NM_000355.3(TCN2):c.-240G>A	rs16988823	0.00004
NM_000355.4(TCN2):c.49C>G (p.Leu17Val)	rs759462885	0.00004
NM_000355.4(TCN2):c.10C>T (p.Leu4Phe)	rs572942248	0.00002
NM_000355.4(TCN2):c.-67C>T	rs1432247695	0.00001
NM_000355.3(TCN2):c.-181A>C	rs2240433
NM_000355.4(TCN2):c.-153C>G	rs886057395
NM_000355.4(TCN2):c.-6G>A	rs771507572
NM_000355.4(TCN2):c.17C>A (p.Ala6Asp)	rs2145528950
NM_000355.4(TCN2):c.19T>C (p.Phe7Leu)
NM_000355.4(TCN2):c.31C>G (p.Leu11Val)	rs2145528995
NM_000355.4(TCN2):c.32T>C (p.Leu11Pro)
NM_000355.4(TCN2):c.44G>A (p.Gly15Glu)
NM_000355.4(TCN2):c.46_47delinsTT (p.Ala16Phe)	rs2145529052
NM_000355.4(TCN2):c.64+4A>T
NM_000355.4(TCN2):c.9C>G (p.His3Gln)	rs1489889957

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