List of variants in gene combination DOCK2, LOC126807589 reported as uncertain significance for immune system 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004946.3(DOCK2):c.854A>G (p.Asn285Ser)	rs762534189	0.00001
NM_004946.3(DOCK2):c.965C>A (p.Pro322His)	rs1673260878	0.00001
NM_004946.3(DOCK2):c.847C>T (p.Leu283Phe)	rs369315365
NM_004946.3(DOCK2):c.866A>G (p.Asn289Ser)	rs1250790966
NM_004946.3(DOCK2):c.896T>C (p.Ile299Thr)
NM_004946.3(DOCK2):c.934_935delinsAA (p.Ala312Lys)	rs1760590564
NM_004946.3(DOCK2):c.947C>T (p.Thr316Met)

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