List of variants in gene combination LOC130004144, RPS24 reported as likely 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_033022.3(RPS24):c.-50G>A	rs190989611	0.00043
NM_033022.4(RPS24):c.-23C>T	rs766457744	0.00002
NM_033022.4(RPS24):c.3+7C>T	rs759947869	0.00001
NM_033022.4(RPS24):c.-37C>T	rs375555593
NM_033022.4(RPS24):c.3+14G>C
NM_033022.4(RPS24):c.3+15G>A	rs764832484
NM_033022.4(RPS24):c.3+16C>T
NM_033022.4(RPS24):c.3+17C>T	rs751476775
NM_033022.4(RPS24):c.3+20T>A
NM_033022.4(RPS24):c.3+7C>G
NM_033022.4(RPS24):c.3+9C>T	rs775865079

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