List of variants in gene combination GSR, LOC130000170 reported as uncertain significance for hematologic disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000637.5(GSR):c.242G>A (p.Arg81His)	rs767823911	0.00003
NM_000637.5(GSR):c.172G>T (p.Ala58Ser)
NM_000637.5(GSR):c.227_253dup (p.Ala84_Glu85insGlyLeuAlaSerAlaArgArgAlaAla)
NM_000637.5(GSR):c.94G>T (p.Glu32Ter)

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