ClinVar Miner

List of variants in gene ARNT2 reported as uncertain significance by New York Genome Center

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_014862.4(ARNT2):c.1414G>A (p.Gly472Ser)	rs138241250	0.00007
NM_014862.4(ARNT2):c.1589C>A (p.Ser530Tyr)	rs771365661	0.00001

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