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rs104894305(C;C)

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common in clinvar

Is a	genotype
of	rs104894305
Gene	SDHD, TIMM8B
Chromosome	11
Position	112,087,899
mentioned	by

0

Good

Geno	Mag	Summary
(A;C)	6.2	Hereditary PGL/PCC Syndrome
(C;C)	0	common in clinvar

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Is a genotype