List of variants in gene SDHC reported as likely pathogenic for Gastrointestinal stromal tumor; 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.215G>A (p.Arg72His)	rs778582853	0.00001
NC_000001.10:g.(?_161326457)_(161326640_?)dup
NC_000001.11:g.(?_161340584)_(161340665_?)dup
NM_003001.5(SDHC):c.148C>A (p.Arg50Ser)
NM_003001.5(SDHC):c.160C>A (p.Pro54Thr)	rs1553262444
NM_003001.5(SDHC):c.171_179+15del	rs1671156558
NM_003001.5(SDHC):c.179+1G>C	rs1057517818
NM_003001.5(SDHC):c.179+1G>T	rs1057517818
NM_003001.5(SDHC):c.179+2T>A
NM_003001.5(SDHC):c.180-2A>G	rs1363265634
NM_003001.5(SDHC):c.20+1G>A
NM_003001.5(SDHC):c.20+1G>T	rs1249046874
NM_003001.5(SDHC):c.20+2T>A
NM_003001.5(SDHC):c.20G>A (p.Arg7Lys)	rs2102271857
NM_003001.5(SDHC):c.224G>A (p.Gly75Asp)	rs786205147
NM_003001.5(SDHC):c.242-1G>A
NM_003001.5(SDHC):c.379C>A (p.His127Asn)	rs1485675090
NM_003001.5(SDHC):c.405+1del	rs1558182956
NM_003001.5(SDHC):c.77+1G>A	rs1558164647

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