List of variants in gene combination LOC126862987, SEC23B reported as uncertain significance for hematologic 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_006363.6(SEC23B):c.519G>A (p.Val173=)	rs138314893	0.00040
NM_006363.6(SEC23B):c.569G>A (p.Arg190Gln)	rs201160833	0.00028
NM_006363.6(SEC23B):c.389T>C (p.Ile130Thr)	rs773290230	0.00008
NM_006363.6(SEC23B):c.436G>A (p.Ala146Thr)	rs2060116077
NM_006363.6(SEC23B):c.501C>G (p.Ile167Met)
NM_006363.6(SEC23B):c.546A>T (p.Gly182=)	rs1347919581
NM_006363.6(SEC23B):c.614G>C (p.Gly205Ala)
NM_006363.6(SEC23B):c.631A>G (p.Met211Val)

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