List of variants in gene SDHD reported by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_003002.4(SDHD):c.315-32T>C	rs4151637	0.11444
NM_003002.4(SDHD):c.170-29A>G	rs9919624	0.11431
NM_003002.4(SDHD):c.204C>T (p.Ser68=)	rs9919552	0.11428
NM_003002.4(SDHD):c.315-1646C>T	rs111659413	0.10719
NM_003002.4(SDHD):c.315-1708C>T	rs113458823	0.02846
NM_003002.4(SDHD):c.312C>T (p.His104=)	rs61734352	0.00690
NM_003002.4(SDHD):c.149A>G (p.His50Arg)	rs11214077	0.00679
NM_003002.4(SDHD):c.435C>T (p.His145=)	rs200062830	0.00002
NM_003002.4(SDHD):c.270G>A (p.Ala90=)	rs766656463	0.00001
NM_003002.4(SDHD):c.169+34_169+37dup
NM_003002.4(SDHD):c.314+3A>C	rs1555187084
NM_003002.4(SDHD):c.315-1686C>A
NM_003002.4(SDHD):c.337_340del (p.Asp113fs)	rs587776648
NM_003002.4(SDHD):c.341A>G (p.Tyr114Cys)	rs104894304

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