ClinVar Miner

List of variants in gene combination LOC126806516, NHEJ1 reported as benign for not specified

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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_024782.3(NHEJ1):c.706+7C>A	rs6720495	0.01626
NM_024782.3(NHEJ1):c.767A>T (p.Gln256Leu)	rs35270667	0.01058

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