List of variants in gene combination INSL6, JAK2 reported as uncertain significance for acute leukemia

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004972.4(JAK2):c.1641+6T>C	rs182123615	0.00103
NM_004972.4(JAK2):c.337C>G (p.Leu113Val)	rs143103233	0.00064
NM_004972.4(JAK2):c.2171T>C (p.Ile724Thr)	rs372254348	0.00013
NM_004972.4(JAK2):c.2768G>A (p.Arg923His)	rs761937412	0.00005
NM_004972.4(JAK2):c.2762-10_2762-9del	rs529050943
NM_004972.4(JAK2):c.2768G>T (p.Arg923Leu)

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