List of variants in gene LRRC8A reported as benign for not provided

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_019594.4(LRRC8A):c.1476T>C (p.Arg492=)	rs3750319	0.60629
NM_019594.4(LRRC8A):c.1014T>C (p.Tyr338=)	rs3750320	0.24050
NM_019594.4(LRRC8A):c.333T>C (p.Ala111=)	rs16930747	0.02968
NM_019594.4(LRRC8A):c.-8-11C>T	rs7860319	0.02689
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.1788G>A (p.Leu596=)	rs116679304	0.00361
NM_019594.4(LRRC8A):c.117C>T (p.Ala39=)	rs75533615	0.00339
NM_019594.4(LRRC8A):c.324C>T (p.Tyr108=)	rs139528042	0.00317
NM_019594.4(LRRC8A):c.267C>T (p.Thr89=)	rs141527072	0.00140
NM_019594.4(LRRC8A):c.1606G>A (p.Val536Ile)	rs138622041	0.00102
NM_019594.4(LRRC8A):c.939C>G (p.Pro313=)	rs369898214	0.00042
NM_019594.4(LRRC8A):c.855C>T (p.Tyr285=)	rs373107119	0.00027
NM_019594.4(LRRC8A):c.1227C>T (p.Asn409=)	rs150061366	0.00022
NM_019594.4(LRRC8A):c.1440G>A (p.Ala480=)	rs143120279	0.00011
NM_019594.4(LRRC8A):c.123C>T (p.Phe41=)	rs375717848	0.00007
NM_019594.4(LRRC8A):c.996C>T (p.Tyr332=)	rs149683863	0.00006
NM_019594.4(LRRC8A):c.918C>T (p.Arg306=)	rs200186109	0.00004
NM_019594.4(LRRC8A):c.1476= (p.Arg492=)

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