List of variants in gene TFAP2B studied for bone development disease

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003221.4(TFAP2B):c.1144C>T (p.Arg382Ter)	rs2113960501
NM_003221.4(TFAP2B):c.3G>A (p.Met1Ile)	rs2113920409
NM_003221.4(TFAP2B):c.601+2T>A	rs2113937986
NM_003221.4(TFAP2B):c.827A>G (p.Lys276Arg)	rs2113952620

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