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rs28931603

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0
Make rs28931603(C;T)
Make rs28931603(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position98580709
GeneCPOX
is asnp
is mentioned by
dbSNPrs28931603
ebirs28931603
HLIrs28931603
Exacrs28931603
Varsomers28931603
Maprs28931603
PheGenIrs28931603
hapmaprs28931603
1000 genomesrs28931603
hgdprs28931603
ensemblrs28931603
gopubmedrs28931603
geneviewrs28931603
scholarrs28931603
googlers28931603
pharmgkbrs28931603
gwascentralrs28931603
openSNPrs28931603
23andMers28931603
23andMe allrs28931603
SNP Nexus

SNPshotrs28931603
SNPdbers28931603
MSV3drs28931603
GWAS Ctlgrs28931603
Max Magnitude0
OMIM121300
DescCOPROPORPHYRIA
Variant0009
Relatedalso
OMIM612732
Desc
Variant0009
Relatedalso


ClinVar
Risk rs28931603(T;T)
Alt rs28931603(T;T)
Reference rs28931603(C;C)
Significance Pathogenic
Disease Coproporphyria
Variation info
Gene CPOX
CLNDBN Coproporphyria
Reversed 1
HGVS NC_000003.11:g.98299553G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000488.2,