List of variants in gene SNTA1 reported as benign for not specified

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_003098.3(SNTA1):c.807T>C (p.Asn269=)	rs73270015	0.02196
NM_003098.3(SNTA1):c.1350C>T (p.Phe450=)	rs116747979	0.01203
NM_003098.3(SNTA1):c.555C>T (p.Val185=)	rs34995247	0.00948
NM_003098.3(SNTA1):c.317G>A (p.Arg106Gln)	rs75025585	0.00904
NM_003098.3(SNTA1):c.166C>T (p.Pro56Ser)	rs573772189	0.00585
NM_003098.3(SNTA1):c.701+10G>A	rs6057846	0.00419
NM_003098.3(SNTA1):c.1426-5T>C	rs183939417	0.00221
NM_003098.3(SNTA1):c.770C>G (p.Ala257Gly)	rs56157422	0.00217
NM_003098.3(SNTA1):c.311-6G>C	rs139532210	0.00201
NM_003098.3(SNTA1):c.221C>T (p.Pro74Leu)	rs572545726	0.00198
NM_003098.3(SNTA1):c.984C>T (p.Pro328=)	rs138863915	0.00121
NM_003098.3(SNTA1):c.497-7C>T	rs116972153	0.00063
NM_003098.3(SNTA1):c.677G>A (p.Cys226Tyr)	rs34479952	0.00037
NM_003098.3(SNTA1):c.909+17G>T	rs376695170	0.00021
NM_003098.3(SNTA1):c.311-20C>T	rs200764326	0.00013
NM_003098.3(SNTA1):c.1238-11C>T	rs779500941	0.00003
NM_003098.3(SNTA1):c.567A>T (p.Ser189=)	rs552315106

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