List of variants in gene KIT reported as likely pathogenic for immune system disorder

Minimum submission review status:		Collection method:
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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_000222.3(KIT):c.1675G>A (p.Val559Ile)	rs121913520
NM_000222.3(KIT):c.2447A>T (p.Asp816Val)	rs121913507
NM_000222.3(KIT):c.2459A>T (p.Asp820Val)	rs121913682
NM_000222.3(KIT):c.2466T>A (p.Asn822Lys)	rs121913514
NM_000222.3(KIT):c.2466T>G (p.Asn822Lys)	rs121913514
NM_000222.3(KIT):c.590C>T (p.Ser197Leu)	rs2109674601

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