List of variants in gene ITGA8 reported as uncertain significance for renal hypodysplasia/aplasia 1

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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_003638.3(ITGA8):c.840T>C (p.Ser280=)	rs151036773	0.00086
NM_003638.3(ITGA8):c.1156T>C (p.Phe386Leu)	rs147384918	0.00011
NM_003638.3(ITGA8):c.158A>G (p.Lys53Arg)	rs1013453104	0.00002
NM_003638.3(ITGA8):c.1159G>A (p.Gly387Ser)
NM_003638.3(ITGA8):c.1961C>T (p.Ser654Leu)
NM_003638.3(ITGA8):c.2075T>A (p.Ile692Lys)

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