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rs121917871

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917871(C;T)
Make rs121917871(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position98593420
GeneCPOX
is asnp
is mentioned by
dbSNPrs121917871
ebirs121917871
HLIrs121917871
Exacrs121917871
Varsomers121917871
Maprs121917871
PheGenIrs121917871
hapmaprs121917871
1000 genomesrs121917871
hgdprs121917871
ensemblrs121917871
gopubmedrs121917871
geneviewrs121917871
scholarrs121917871
googlers121917871
pharmgkbrs121917871
gwascentralrs121917871
openSNPrs121917871
23andMers121917871
23andMe allrs121917871
SNP Nexus

SNPshotrs121917871
SNPdbers121917871
MSV3drs121917871
GWAS Ctlgrs121917871
Max Magnitude0
ClinVar
Risk rs121917871(T;T)
Alt rs121917871(T;T)
Reference rs121917871(C;C)
Significance Pathogenic
Disease Coproporphyria
Variation info
Gene CPOX
CLNDBN Coproporphyria
Reversed 1
HGVS NC_000003.11:g.98312264G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000487.3,