List of variants in gene MAP3K1 reported as uncertain significance by GeneDx

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005921.2(MAP3K1):c.3070A>C (p.Lys1024Gln)	rs780666910	0.00003
NM_005921.2(MAP3K1):c.2668C>T (p.Pro890Ser)	rs777039063
NM_005921.2(MAP3K1):c.3062C>T (p.Thr1021Ile)	rs901499471
NM_005921.2(MAP3K1):c.868G>T (p.Ala290Ser)	rs2530908380
NM_005921.2(MAP3K1):c.963G>T (p.Gln321His)	rs377226281

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