List of variants in gene SNTA1 reported as uncertain significance by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.440C>A (p.Thr147Asn)	rs141724500	0.00067
NM_003098.3(SNTA1):c.787G>T (p.Ala263Ser)	rs150576530	0.00054
NM_003098.3(SNTA1):c.784A>C (p.Thr262Pro)	rs200316080	0.00041
NM_003098.3(SNTA1):c.375G>C (p.Gln125His)	rs201421292	0.00001
NM_003098.3(SNTA1):c.544G>A (p.Gly182Arg)	rs201405395	0.00001
NM_003098.3(SNTA1):c.1057C>G (p.Pro353Ala)	rs786205427
NM_003098.3(SNTA1):c.1330G>A (p.Val444Met)	rs201571071
NM_003098.3(SNTA1):c.1498C>T (p.Arg500Cys)	rs786205426
NM_003098.3(SNTA1):c.845T>A (p.Leu282Gln)	rs200878531

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