List of variants in gene LOC126861339, SDHD studied for developmental defect during embryogenesis

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003002.4(SDHD):c.34G>A (p.Gly12Ser)	rs34677591	0.00706
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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