List of variants in gene DOCK2, LOC126807589 studied for immune system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_004946.3(DOCK2):c.844-4C>A	rs3734099	0.17712
NM_004946.3(DOCK2):c.979+11C>T	rs116819880	0.00185
NM_004946.3(DOCK2):c.979+6G>A	rs200237259	0.00051
NM_004946.3(DOCK2):c.844-8C>T	rs553926409	0.00006
NM_004946.3(DOCK2):c.979+19A>G	rs749750176	0.00003
NM_004946.3(DOCK2):c.972G>A (p.Gly324=)	rs757457405	0.00002
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.844-3del	rs1281812557
NM_004946.3(DOCK2):c.844-7C>T
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.906C>G (p.Val302=)	rs146489287
NM_004946.3(DOCK2):c.906C>T (p.Val302=)	rs146489287
NM_004946.3(DOCK2):c.934_935delinsAA (p.Ala312Lys)	rs1760590564
NM_004946.3(DOCK2):c.947C>T (p.Thr316Met)
NM_004946.3(DOCK2):c.979+7G>A
NM_004946.3(DOCK2):c.979+8G>A

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