ClinVar Miner

List of variants in gene combination LOC132089454, SLC17A5 reported by Counsyl

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_012434.5(SLC17A5):c.292-1G>C	rs1554164322
NM_012434.5(SLC17A5):c.292-2A>C	rs1057516528
NM_012434.5(SLC17A5):c.349dup (p.Tyr117fs)	rs772039085

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