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rs267606803

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606803(A;A)
Make rs267606803(A;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position57550760
GeneFECH
is asnp
is mentioned by
dbSNPrs267606803
ebirs267606803
HLIrs267606803
Exacrs267606803
Varsomers267606803
Maprs267606803
PheGenIrs267606803
hapmaprs267606803
1000 genomesrs267606803
hgdprs267606803
ensemblrs267606803
gopubmedrs267606803
geneviewrs267606803
scholarrs267606803
googlers267606803
pharmgkbrs267606803
gwascentralrs267606803
openSNPrs267606803
23andMers267606803
23andMe allrs267606803
SNP Nexus

SNPshotrs267606803
SNPdbers267606803
MSV3drs267606803
GWAS Ctlgrs267606803
Max Magnitude0
ClinVar
Risk rs267606803(A;A)
Alt rs267606803(A;A)
Reference rs267606803(T;T)
Significance Pathogenic
Disease Erythropoietic protoporphyria
Variation info
Gene FECH
CLNDBN Erythropoietic protoporphyria
Reversed 1
HGVS NC_000018.9:g.55217992A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000591.3,