List of variants in gene combination LINC00630, RAB40AL reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001031834.1(RAB40AL):c.82A>G (p.Ser28Gly)	rs61745026	0.15414
NM_001031834.1(RAB40AL):c.69G>C (p.Arg23Ser)	rs61745030	0.15369
NM_001031834.1(RAB40AL):c.447C>T (p.Gly149=)	rs7066794	0.11958
NM_001031834.1(RAB40AL):c.435C>T (p.Ala145=)	rs61745022	0.11180
NM_001031834.1(RAB40AL):c.639G>A (p.Pro213=)	rs7876193	0.01629
NM_001031834.1(RAB40AL):c.126G>A (p.Pro42=)	rs61745023	0.01604
NM_001031834.1(RAB40AL):c.279C>T (p.Val93=)	rs201052380	0.00059

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