List of variants in gene LRRC8A reported as likely benign for hematologic disorder

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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_019594.4(LRRC8A):c.1458C>T (p.Pro486=)	rs11999276	0.01838
NM_019594.4(LRRC8A):c.1699G>A (p.Val567Met)	rs143836544	0.00321
NM_019594.4(LRRC8A):c.1606G>A (p.Val536Ile)	rs138622041	0.00102
NM_019594.4(LRRC8A):c.33G>A (p.Ala11=)	rs202218761	0.00011
NM_019594.4(LRRC8A):c.1586C>T (p.Ala529Val)	rs150164316	0.00004
NM_019594.4(LRRC8A):c.203C>T (p.Ser68Leu)	rs147311433	0.00002

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