List of variants in gene combination LOC130065680, SNTA1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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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_003098.3(SNTA1):c.128G>A (p.Ser43Asn)	rs786205841	0.00022
NM_003098.3(SNTA1):c.40G>A (p.Glu14Lys)	rs786205846	0.00014
NM_003098.3(SNTA1):c.-261C>A	rs536994978	0.00010
NM_003098.3(SNTA1):c.-262C>T	rs550104436	0.00010
NM_003098.3(SNTA1):c.101G>A (p.Ser34Asn)	rs963277918	0.00009
NM_003098.3(SNTA1):c.25C>T (p.Arg9Cys)	rs886039012	0.00002

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