List of variants in gene EXOC6B reported as pathogenic for bone development disease

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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: 4

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HGVS	dbSNP	gnomAD frequency
NG_050967.1:g.291668_510915del
NM_015189.1:c.2122+15447_2197-59588del
NM_015189.3(EXOC6B):c.401T>G (p.Leu134Ter)	rs2104774484
NM_015189.3(EXOC6B):c.906T>A (p.Tyr302Ter)	rs1294100541

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