Variants in gene JAK3 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_000215.4(JAK3):c.394C>A (p.Pro132Thr)	rs3212723	0.02676
NM_000215.4(JAK3):c.2164G>A (p.Val722Ile)	rs3213409	0.00743
NM_000215.4(JAK3):c.452C>G (p.Pro151Arg)	rs55778349	0.00647
NM_000215.4(JAK3):c.631A>C (p.Arg211=)	rs56269787	0.00207
NM_000215.4(JAK3):c.108G>C (p.Gly36=)	rs149701114	0.00201
NM_000215.4(JAK3):c.1131C>T (p.His377=)	rs55802448	0.00098
NM_000215.4(JAK3):c.3300C>T (p.Ser1100=)	rs201073968	0.00041
NM_000215.4(JAK3):c.2235G>A (p.Pro745=)	rs149207170	0.00026
NM_000215.4(JAK3):c.1843C>T (p.Arg615Cys)	rs200075643	0.00002
NM_000215.4(JAK3):c.2451C>T (p.Phe817=)	rs201576913	0.00001

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