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rs137854448(C;T)

From SNPedia
Maybe: Severe congenital neutropenia, type 1, autosomal dominant; see discussion
Is agenotype
ofrs137854448
GeneELANE
Chromosome19
Position855,613
Merged fromRs28929493
mentionedby
Magnitude8.2
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 8.2 Maybe: Severe congenital neutropenia, type 1, autosomal dominant; see discussion

23andMe appears to overcall this location in individuals who do not have any form of neutropenia, however if you're seeing this in your report you probably weren't tested by 23andMe. Please contact us (info@snpedia.com) if your data indicates you have this genotype and you are willing to indicate if you have any form of neutropenia. Additional discussion at rs137854448.