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

rs1800435(C;G)

From SNPedia
Carrier of an ALAD deficiency porphyria mutation
Is agenotype
ofrs1800435
GeneALAD
Chromosome9
Position113,391,611
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;G) 3 Carrier of an ALAD deficiency porphyria mutation
(G;G) 0 common in clinvar

Unaffected in absence of a second mutation in the ALAD gene; see links via main rs-page and the ALAD gene page