List of variants in gene VPS13A reported as benign by Athena Diagnostics Inc

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_033305.3(VPS13A):c.9069A>G (p.Gly3023=)	rs3737289	0.40290
NM_033305.3(VPS13A):c.6492T>C (p.Asp2164=)	rs7025532	0.18911
NM_033305.3(VPS13A):c.8571T>C (p.Tyr2857=)	rs17340192	0.05788
NM_033305.3(VPS13A):c.5583A>G (p.Thr1861=)	rs17423984	0.05526
NM_033305.3(VPS13A):c.9027A>G (p.Pro3009=)	rs17081163	0.01458
NM_033305.3(VPS13A):c.9370C>A (p.His3124Asn)	rs117983287	0.00817
NM_033305.3(VPS13A):c.8676C>T (p.Ile2892=)	rs117485827	0.00672
NM_033305.3(VPS13A):c.5625A>G (p.Leu1875=)	rs146280301	0.00643
NM_033305.3(VPS13A):c.7053T>C (p.Ala2351=)	rs139753431	0.00641
NM_033305.3(VPS13A):c.6410A>G (p.Glu2137Gly)	rs114232513	0.00574
NM_033305.3(VPS13A):c.5673G>A (p.Ser1891=)	rs114699935	0.00559
NM_033305.3(VPS13A):c.5979C>T (p.Arg1993=)	rs41289971	0.00487
NM_033305.3(VPS13A):c.5184T>C (p.Ser1728=)	rs73467954	0.00400
NM_033305.3(VPS13A):c.2748A>G (p.Glu916=)	rs73466090	0.00324
NM_033305.3(VPS13A):c.1758T>C (p.Ala586=)	rs149037185	0.00199
NM_033305.3(VPS13A):c.3078T>G (p.Thr1026=)	rs141835897	0.00171
NM_033305.3(VPS13A):c.6690C>T (p.Asp2230=)	rs139115188	0.00115

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