List of variants in gene combination LOC129992625, SRP72 reported as uncertain significance for hematologic disorder

Minimum submission review status:		Collection method:
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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006947.4(SRP72):c.29C>T (p.Ser10Leu)	rs752240949	0.00001
NM_006947.4(SRP72):c.7A>G (p.Ser3Gly)	rs1719782337	0.00001
NM_006947.4(SRP72):c.-10C>T

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