List of variants in gene TELO2 reported as uncertain significance for multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_016111.4(TELO2):c.238C>A (p.His80Asn)	rs199863486	0.00014
NM_016111.4(TELO2):c.1129C>T (p.Arg377Trp)	rs200293618	0.00012
NM_016111.4(TELO2):c.2296G>A (p.Val766Met)	rs371675497	0.00010
NM_016111.4(TELO2):c.392G>A (p.Gly131Asp)	rs187225056	0.00006
NM_016111.4(TELO2):c.1747G>A (p.Val583Ile)	rs775272837	0.00004
NM_016111.4(TELO2):c.2003G>A (p.Arg668Gln)	rs150934316	0.00001
NM_016111.4(TELO2):c.1382C>T (p.Thr461Met)	rs199748546
NM_016111.4(TELO2):c.1476T>G (p.Asp492Glu)	rs2039707751
NM_016111.4(TELO2):c.1546C>T (p.Arg516Trp)
NM_016111.4(TELO2):c.2002C>T (p.Arg668Trp)
NM_016111.4(TELO2):c.2449G>A (p.Ala817Thr)	rs2040070431
NM_016111.4(TELO2):c.340A>C (p.Ser114Arg)
NM_016111.4(TELO2):c.490C>T (p.Pro164Ser)
NM_016111.4(TELO2):c.925C>T (p.Arg309Trp)
NM_016111.4(TELO2):c.967G>C (p.Ala323Pro)	rs750187494

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