Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1042503(A;G)

From SNPedia
Benign polymorphism (likely)
Is agenotype
ofrs1042503
GenePAH
Chromosome12
Position102,852,922
mentionedby
Magnitude1
ReputeGood
Geno Mag Summary
(A;G) 1 Benign polymorphism (likely)
(G;G) 0 common in clinvar

ClinVar tag of pathogenic is misleading; it refers to an allele that carries another mutation. This SNP is a synonymous variant.