List of variants in gene combination LOC121853040, TCN2 reported as likely benign for immune system disorder

Minimum submission review status:		Collection method:
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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000355.3(TCN2):c.-250C>T	rs5753231	0.14215
NM_000355.4(TCN2):c.64+13C>T	rs370228236	0.00006
NM_000355.4(TCN2):c.18C>T (p.Ala6=)
NM_000355.4(TCN2):c.21C>T (p.Phe7=)
NM_000355.4(TCN2):c.24C>G (p.Leu8=)
NM_000355.4(TCN2):c.27C>T (p.Phe9=)
NM_000355.4(TCN2):c.30T>A (p.Leu10=)	rs2145528985
NM_000355.4(TCN2):c.33G>A (p.Leu11=)
NM_000355.4(TCN2):c.54T>C (p.Thr18=)
NM_000355.4(TCN2):c.57G>A (p.Glu19=)
NM_000355.4(TCN2):c.64+12G>A
NM_000355.4(TCN2):c.64+14C>T
NM_000355.4(TCN2):c.64+15T>C
NM_000355.4(TCN2):c.64+16C>G	rs2145529135
NM_000355.4(TCN2):c.64+18A>G
NM_000355.4(TCN2):c.64+19T>A
NM_000355.4(TCN2):c.64+20C>T
NM_000355.4(TCN2):c.64+9C>T

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