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rs387906553(A;G)

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Revision as of 19:09, 28 November 2018 by Lennon (talk | contribs)
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Possible miscall in Ancestry v2 data; otherwise, severe congenital neutropenia, type 1, autosomal dominant
Is agenotype
ofrs387906553
GeneELANE
Chromosome19
Position853,022
mentionedby
Magnitude8.2
ReputeBad
Geno Mag Summary
(A;G) 8.2 Possible miscall in Ancestry v2 data; otherwise, severe congenital neutropenia, type 1, autosomal dominant
(G;G) 0 common in clinvar

see links at rs387906553