ClinVar Miner

List of variants in gene combination GALK1, ITGB4 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000213.5(ITGB4):c.4462C>T (p.Leu1488Phe)	rs548288813	0.00004
NM_000213.5(ITGB4):c.4364C>T (p.Thr1455Ile)	rs554267559

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