ClinVar Miner

List of variants in gene combination HRAS, LRRC56 reported as uncertain significance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.257A>C (p.Asn86Thr)	rs138272051	0.00019
NM_005343.4(HRAS):c.108dup (p.Glu37fs)	rs2133994149

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