ClinVar Miner

List of variants in gene SARM1 reported as uncertain significance

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015077.4(SARM1):c.1501T>C (p.Tyr501His)	rs144613221	0.00178
NM_015077.4(SARM1):c.25G>C (p.Ala9Pro)	rs1224579416	0.00001

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