List of variants in gene TTC21A studied for spermatogenic failure

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001366900.1(TTC21A):c.3095+5G>T	rs148431487	0.00058
NM_001366900.1(TTC21A):c.341A>G (p.Tyr114Cys)	rs750057655	0.00002
NM_001366900.1(TTC21A):c.2308C>T (p.Gln770Ter)	rs780431020
NM_001366900.1(TTC21A):c.2542del (p.Ala847_Val848insTer)	rs1559708295
NM_001366900.1(TTC21A):c.716+1G>A	rs1559674534

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