List of variants in gene LRRC8A reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_019594.4(LRRC8A):c.1509C>T (p.Thr503=)	rs3750318	0.02605
NM_019594.4(LRRC8A):c.1458C>T (p.Pro486=)	rs11999276	0.01838
NM_019594.4(LRRC8A):c.2118C>G (p.Leu706=)	rs35266233	0.01461
NM_019594.4(LRRC8A):c.2157+11C>T	rs11999754	0.01366
NM_019594.4(LRRC8A):c.1803T>C (p.Cys601=)	rs16930757	0.01361
NM_019594.4(LRRC8A):c.51C>T (p.Tyr17=)	rs16930745	0.00880
NM_019594.4(LRRC8A):c.774C>T (p.Asp258=)	rs41275930	0.00741
NM_019594.4(LRRC8A):c.1995G>A (p.Glu665=)	rs11999752	0.00533
NM_019594.4(LRRC8A):c.1371C>T (p.Pro457=)	rs11999256	0.00516
NM_019594.4(LRRC8A):c.1606G>A (p.Val536Ile)	rs138622041	0.00102
NM_019594.4(LRRC8A):c.-2C>T

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