List of variants in gene SDHC reported as uncertain significance for Gastrointestinal stromal tumor; Carney-Stratakis syndrome; Paragangliomas 3

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.98C>T (p.Thr33Met)	rs148566767	0.00007
NM_003001.5(SDHC):c.11T>C (p.Leu4Pro)	rs774299337	0.00001
NM_003001.5(SDHC):c.128A>G (p.Asn43Ser)	rs747349777	0.00001
NM_003001.5(SDHC):c.25G>A (p.Val9Ile)	rs774768866	0.00001
NM_003001.5(SDHC):c.263C>T (p.Ser88Leu)	rs778212096	0.00001
NM_003001.5(SDHC):c.436C>A (p.Pro146Thr)	rs541660851	0.00001
NM_003001.5(SDHC):c.54T>G (p.Phe18Leu)	rs200761743	0.00001
NM_003001.5(SDHC):c.82G>T (p.Val28Phe)	rs754818119	0.00001
NM_003001.5(SDHC):c.160C>A (p.Pro54Thr)	rs1553262444
NM_003001.5(SDHC):c.356C>T (p.Ala119Val)
NM_003001.5(SDHC):c.422A>G (p.Lys141Arg)	rs1558185879
NM_003001.5(SDHC):c.4G>C (p.Ala2Pro)	rs1198315342
NM_003001.5(SDHC):c.7G>T (p.Ala3Ser)	rs748243732

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