List of variants in gene combination LOC130004025, SLC29A3 reported as uncertain significance for immune system 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_018344.6(SLC29A3):c.-23C>T	rs771479944	0.00016
NM_018344.6(SLC29A3):c.-31G>C	rs886047116	0.00002
NC_000010.10:g.(?_73079047)_(73082831_?)dup

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