List of variants in gene SLC37A4 reported as not provided for leukopenia

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001164277.2(SLC37A4):c.1042_1043del (p.Leu348fs)	rs80356491	0.00026
NM_001164277.2(SLC37A4):c.1015G>T (p.Gly339Cys)	rs80356490	0.00008
NM_001164277.2(SLC37A4):c.352T>C (p.Trp118Arg)	rs80356489	0.00001

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