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

rs121917866

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917866(C;T)
Make rs121917866(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position98585622
GeneCPOX
is asnp
is mentioned by
dbSNPrs121917866
ebirs121917866
HLIrs121917866
Exacrs121917866
Varsomers121917866
Maprs121917866
PheGenIrs121917866
hapmaprs121917866
1000 genomesrs121917866
hgdprs121917866
ensemblrs121917866
gopubmedrs121917866
geneviewrs121917866
scholarrs121917866
googlers121917866
pharmgkbrs121917866
gwascentralrs121917866
openSNPrs121917866
23andMers121917866
23andMe allrs121917866
SNP Nexus

SNPshotrs121917866
SNPdbers121917866
MSV3drs121917866
GWAS Ctlgrs121917866
Max Magnitude0
ClinVar
Risk rs121917866(T;T)
Alt rs121917866(T;T)
Reference rs121917866(C;C)
Significance Pathogenic
Disease Coproporphyria
Variation info
Gene CPOX
CLNDBN Coproporphyria
Reversed 1
HGVS NC_000003.11:g.98304466G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000480.2,