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rs1763442

From SNPedia

Merged intors1144520
Orientationplus
Make rs1763442(A;A)
Make rs1763442(A;T)
Make rs1763442(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position29097084
is asnp
is mentioned by
dbSNPrs1763442
ebirs1763442
HLIrs1763442
Exacrs1763442
Varsomers1763442
Maprs1763442
PheGenIrs1763442
hapmaprs1763442
1000 genomesrs1763442
hgdprs1763442
ensemblrs1763442
gopubmedrs1763442
geneviewrs1763442
scholarrs1763442
googlers1763442
pharmgkbrs1763442
gwascentralrs1763442
openSNPrs1763442
23andMers1763442
23andMe allrs1763442
SNP Nexus

SNPshotrs1763442
SNPdbers1763442
MSV3drs1763442
GWAS Ctlgrs1763442
StatusMerged into rs1144520
Max Magnitude
The ferrochelatase FECH gene is involved in the metabolism of heme. Deficiencies of the enzyme can cause erythropoietic protoporphyria, a type of photosensitivity that can cause serious skin reactions.[1] This inherited condition has incomplete penetrance.