List of variants in gene combination LOC129929542, SDHB reported as uncertain significance for Gastrointestinal stromal tumor

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.50C>T (p.Thr17Ile)	rs138979875	0.00001
NM_003000.3(SDHB):c.65G>A (p.Cys22Tyr)	rs141230910
NM_003000.3(SDHB):c.67C>G (p.Leu23Val)	rs1553179319
NM_003000.3(SDHB):c.71_72delinsCC (p.Gln24Pro)	rs2078163018
NM_003000.3(SDHB):c.72+5G>A	rs878854581

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