List of variants in gene RHOA reported as likely pathogenic for Carcinoma of esophagus

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001664.4(RHOA):c.13C>T (p.Arg5Trp)	rs1057519952
NM_001664.4(RHOA):c.14G>A (p.Arg5Gln)	rs1057519953
NM_001664.4(RHOA):c.14G>T (p.Arg5Leu)	rs1057519953

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