List of variants in gene SLC6A9 reported as likely pathogenic for inborn disorder of serine family metabolism

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_001024845.3(SLC6A9):c.1536+1G>A
NM_001024845.3(SLC6A9):c.235C>T (p.Pro79Ser)	rs2154305890
NM_001024845.3(SLC6A9):c.31-6164G>C	rs2154306852

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