List of variants in gene combination LOC129992625, SRP72 reported as benign for anemia

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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_006947.4(SRP72):c.19G>T (p.Gly7Trp)	rs17524437
NM_006947.4(SRP72):c.20G>A (p.Gly7Glu)	rs139502866
NM_006947.4(SRP72):c.20G>C (p.Gly7Ala)	rs139502866
NM_006947.4(SRP72):c.21G>T (p.Gly7=)	rs12513091
NM_006947.4(SRP72):c.23G>A (p.Gly8Glu)	rs760960779

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