List of variants in gene combination GOSR2, LRRC37A2 reported as benign for brain disorder

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004287.5(GOSR2):c.*301T>C	rs8078556	0.93627
NM_004287.5(GOSR2):c.*2337T>C	rs1052586	0.48306
NM_004287.5(GOSR2):c.*1519T>C	rs4968286	0.44908
NM_004287.5(GOSR2):c.*1733A>G	rs758392	0.41414
NM_004287.5(GOSR2):c.*1115G>A	rs758391	0.38725
NM_004287.5(GOSR2):c.94+7A>C	rs376231923	0.00016
NM_004287.5(GOSR2):c.*1711G>A	rs11657819
NM_004287.5(GOSR2):c.-12G>C	rs183199
NM_004287.5(GOSR2):c.-30G>C	rs189899
NM_004287.5(GOSR2):c.437A>G (p.Asn146Ser)
NM_004287.5(GOSR2):c.477+19del	rs755765859
NM_004287.5(GOSR2):c.7C>A (p.Pro3Thr)	rs12944167

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