List of variants in gene SPTLC1 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006415.4(SPTLC1):c.*124A>G	rs189582528	0.00666
NM_006415.4(SPTLC1):c.1411G>A (p.Val471Ile)	rs141292904	0.00272
NM_006415.4(SPTLC1):c.985-5C>T	rs114380004	0.00245
NM_006415.4(SPTLC1):c.427+446C>T

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