List of variants in gene combination DOCK8, LOC130001437 reported as likely benign 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.52A>G (p.Arg18Gly)	rs200689054	0.00103
NM_203447.4(DOCK8):c.6C>T (p.Ala2=)	rs759932577	0.00003
NM_203447.4(DOCK8):c.12G>T (p.Leu4=)	rs753215803	0.00001
NM_203447.4(DOCK8):c.10C>T (p.Leu4=)	rs1237906578
NM_203447.4(DOCK8):c.18C>T (p.Ser6=)
NM_203447.4(DOCK8):c.27C>G (p.Arg9=)	rs1465766530
NM_203447.4(DOCK8):c.33G>A (p.Ala11=)
NM_203447.4(DOCK8):c.36C>A (p.Phe12Leu)	rs566738926
NM_203447.4(DOCK8):c.36C>G (p.Phe12Leu)	rs566738926
NM_203447.4(DOCK8):c.39G>A (p.Ala13=)
NM_203447.4(DOCK8):c.48C>T (p.Ile16=)

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