List of variants in gene combination INSL6, JAK2 reported as likely pathogenic for bone cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004972.4(JAK2):c.1849G>T (p.Val617Phe)	rs77375493	0.00036
NM_004972.4(JAK2):c.1691G>T (p.Arg564Leu)	rs368927897
NM_004972.4(JAK2):c.2047A>G (p.Arg683Gly)	rs1057519721
NM_004972.4(JAK2):c.2624C>A (p.Thr875Asn)	rs1057520016

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