Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894182(A;G)

From SNPedia
(Redirected from I5000833(C;T))
Carrier of a hemophagocytic lymphohistiocytosis (HLH) mutation
Is agenotype
ofrs104894182
GenePRF1
Chromosome10
Position70,598,885
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;G) 3 Carrier of a hemophagocytic lymphohistiocytosis (HLH) mutation
(G;G) 0 common in clinvar

Unaffected in absence of a second PRF1 gene mutation; see links via main rs-page.