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rs3848519(A;A)

From SNPedia
likely to be a benign variant
Is agenotype
ofrs3848519
GeneFECH
Chromosome18
Position57,580,104
mentionedby
Magnitude1
Geno Mag Summary
(A;A) 1 likely to be a benign variant
(A;C) 1 likely to be a benign variant
(C;C) 0 common in complete genomics