List of variants in gene TELO2 reported as likely pathogenic for not provided

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_016111.4(TELO2):c.2296G>A (p.Val766Met)	rs371675497	0.00010
NM_016111.4(TELO2):c.2312T>C (p.Leu771Ser)	rs201230315	0.00009
NM_016111.4(TELO2):c.392G>A (p.Gly131Asp)	rs187225056	0.00006
NM_016111.4(TELO2):c.1826G>A (p.Arg609His)	rs754162070	0.00001
NM_016111.4(TELO2):c.1110del (p.Gln370fs)	rs2141037423
NM_016111.4(TELO2):c.1A>T (p.Met1Leu)
NM_016111.4(TELO2):c.2227-1G>A
NM_016111.4(TELO2):c.2291+1G>A	rs76038845
NM_016111.4(TELO2):c.2291+1G>C	rs76038845
NM_016111.4(TELO2):c.2299C>T (p.Arg767Cys)
NM_016111.4(TELO2):c.561del (p.Leu188fs)	rs1555469732
NM_016111.4(TELO2):c.742_830+600del	rs2505926819

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