List of variants in gene SLC52A1 reported as pathogenic for nutritional deficiency disease

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_017986.4(SLC52A1):c.1134+11G>A	rs141935493	0.00204
NG_033117.2:g.(12554_12700)_(13936_14029)del
Single allele

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