List of variants in gene combination GOSR2, LRRC37A2 reported as benign by GeneDx

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_004287.5(GOSR2):c.337-147T>G	rs169126	0.99997
NM_004287.5(GOSR2):c.*301T>C	rs8078556	0.93627
NM_004287.5(GOSR2):c.94+263A>G	rs2072317	0.62802
NM_004287.5(GOSR2):c.*1519T>C	rs4968286	0.44908
NM_004287.5(GOSR2):c.337-308A>G	rs197926	0.42864
NM_004287.5(GOSR2):c.*1733A>G	rs758392	0.41414
NM_004287.5(GOSR2):c.478-130T>C	rs7221042	0.10690
NM_004287.5(GOSR2):c.94+257C>G	rs75921757	0.07941
NM_004287.5(GOSR2):c.29+149C>T	rs12150668	0.04113
NM_004287.5(GOSR2):c.*1655A>G	rs116123534	0.03006
NM_004287.5(GOSR2):c.29+114A>G	rs111850322	0.01872
NC_000017.11:g.46922988C>T	rs76374478	0.01722
NM_004287.5(GOSR2):c.94+153T>G	rs16941285	0.01546
NM_004287.5(GOSR2):c.40G>A (p.Glu14Lys)	rs113817924	0.00232
NM_004287.5(GOSR2):c.-16C>G	rs373192791	0.00227
NM_004287.5(GOSR2):c.369A>G (p.Ser123=)	rs150381512	0.00064
NM_004287.5(GOSR2):c.-23C>A	rs562237021	0.00041
NM_004287.5(GOSR2):c.29+8C>T	rs573306680	0.00029
NM_004287.5(GOSR2):c.-26G>C	rs369892885	0.00021
NM_004287.5(GOSR2):c.94+7A>C	rs376231923	0.00016
NM_004287.5(GOSR2):c.336+9G>A	rs200210055	0.00013
NM_001012511.3(GOSR2):c.-32_-31insCCAGAGCCAG	rs779892743
NM_004287.5(GOSR2):c.*1711G>A	rs11657819
NM_004287.5(GOSR2):c.288_296dup	rs376212419
NM_004287.5(GOSR2):c.-12G>C	rs183199
NM_004287.5(GOSR2):c.-30G>C	rs189899
NM_004287.5(GOSR2):c.336+45G>T	rs16941300
NM_004287.5(GOSR2):c.478-20dup	rs552913709
NM_004287.5(GOSR2):c.7C>A (p.Pro3Thr)	rs12944167

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