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rs121908917(C;C)

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common in clinvar

Is a	genotype
of	rs121908917
Gene	SCN9A, LOC101929680
Chromosome	2
Position	166,293,354
mentioned	by

0

Good

Geno	Mag	Summary
(A;A)	4	Congenital insensitivity to pain
(A;C)	3	carrier of one allele for insensitivity to pain
(C;C)	0	common in clinvar

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Is a genotype