List of variants in gene TAF2 reported as likely pathogenic for multiple congenital anomalies/dysmorphic syndrome-intellectual disability

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003184.4(TAF2):c.2531C>T (p.Pro844Leu)	rs750451843	0.00002
NM_003184.4(TAF2):c.2380T>A (p.Tyr794Asn)	rs2131063622

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