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rs1800556(C;C)

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common in clinvar

Is a	genotype
of	rs1800556
Gene	ACADS
Chromosome	12
Position	120,737,875
Merged from	Rs28940873
mentioned	by

0

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	1.5	Considered to be a 'susceptibility' variant by some for SCAD; see text

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Is a genotype