ClinVar Miner

List of variants in gene combination LOC130009747, SUCLA2 reported by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003850.3(SUCLA2):c.90+24G>A	rs9567972	0.71583
NM_003850.3(SUCLA2):c.90+76G>C	rs7982426	0.06060
NM_003850.3(SUCLA2):c.45C>T (p.Thr15=)	rs35899901	0.00624

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