List of variants in gene ZNF462 reported as benign for bone disorder

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_021224.6(ZNF462):c.5483A>G (p.Asn1828Ser)	rs3814538	0.49773
NM_021224.6(ZNF462):c.3666T>C (p.Asn1222=)	rs3814540	0.45791
NM_021224.6(ZNF462):c.1210A>G (p.Met404Val)	rs17723637	0.12751
NM_021224.6(ZNF462):c.3559C>T (p.Pro1187Ser)	rs3814541	0.11138
NM_021224.6(ZNF462):c.5328G>A (p.Ser1776=)	rs17785570	0.00871
NM_021224.6(ZNF462):c.5254G>A (p.Asp1752Asn)	rs141348266	0.00045

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