List of variants in gene combination LOC126861339, SDHD reported as uncertain significance for hereditary skeletal muscle 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003002.4(SDHD):c.35G>A (p.Gly12Asp)	rs764384503	0.00001
NM_003002.4(SDHD):c.28G>A (p.Val10Ile)	rs1555186671

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