List of variants in gene SDHD studied for not specified

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_003002.4(SDHD):c.*613T>C	rs693441	0.93280
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.*803A>G	rs17113461	0.10714
NM_003002.4(SDHD):c.*260T>A	rs149570245	0.04112
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.*428A>G	rs184654032	0.00590
NM_003002.4(SDHD):c.*822T>C	rs201472512	0.00133
NM_003002.4(SDHD):c.278A>G (p.Tyr93Cys)	rs142135772	0.00049
NM_003002.4(SDHD):c.101T>G (p.Phe34Cys)	rs141802836	0.00016
NM_003002.4(SDHD):c.255G>C (p.Leu85Phe)	rs199517389	0.00013
NM_003002.4(SDHD):c.116C>T (p.Pro39Leu)	rs752689382	0.00002
NM_003002.4(SDHD):c.438T>C (p.Asp146=)	rs201328474	0.00002
NM_003002.4(SDHD):c.479G>T (p.Ter160Leu)	rs201372601	0.00002
NM_003002.4(SDHD):c.217A>G (p.Ser73Gly)	rs748545223	0.00001
NM_003002.4(SDHD):c.335C>T (p.Thr112Ile)	rs199869408	0.00001
NM_003002.4(SDHD):c.255G>T (p.Leu85Phe)	rs199517389
NM_003002.4(SDHD):c.269C>T (p.Ala90Val)	rs200255724
NM_003002.4(SDHD):c.281C>T (p.Ser94Phe)	rs199754684
NM_003002.4(SDHD):c.314+20del	rs755475561
NM_003002.4(SDHD):c.315-1686C>A
NM_003002.4(SDHD):c.342T>A (p.Tyr114Ter)	rs1050032491
NM_003002.4(SDHD):c.480A>G (p.Ter160Trp)	rs587778663
NM_003002.4(SDHD):c.53-52_53-49del	rs562618773
NM_003002.4(SDHD):c.91A>G (p.Ile31Val)	rs1865653068

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