List of variants in gene SLC44A1 reported as benign

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_080546.5(SLC44A1):c.*862G>A	rs2771040	0.79264
NM_080546.5(SLC44A1):c.1930T>G (p.Ser644Ala)	rs3199966	0.18199
NM_080546.5(SLC44A1):c.966C>T (p.His322=)	rs143807755	0.00038
NM_080546.5(SLC44A1):c.1701A>G (p.Val567=)	rs575344705	0.00035
NM_080546.5(SLC44A1):c.670+9T>C	rs201664137	0.00028
NM_001330731.2(SLC44A1):c.1951-9T>C
NM_080546.5(SLC44A1):c.954C>A (p.Ile318=)	rs139580101

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