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rs137854448(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs137854448
GeneELANE
Chromosome19
Position855,613
Merged fromRs28929493
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 8.2 Maybe: Severe congenital neutropenia, type 1, autosomal dominant; see discussion