List of variants in gene GNA11 reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002067.5(GNA11):c.1018G>A (p.Val340Met)	rs2145329230
NM_002067.5(GNA11):c.179G>T (p.Arg60Leu)	rs587777707
NM_002067.5(GNA11):c.547C>T (p.Arg183Cys)	rs1555702147
NM_002067.5(GNA11):c.626A>G (p.Gln209Arg)	rs1057519742
NM_002067.5(GNA11):c.626A>T (p.Gln209Leu)	rs1057519742

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