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rs121918063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918063(G;G)
Make rs121918063(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position45013928
GeneUROD
is asnp
is mentioned by
dbSNPrs121918063
ebirs121918063
HLIrs121918063
Exacrs121918063
Varsomers121918063
Maprs121918063
PheGenIrs121918063
hapmaprs121918063
1000 genomesrs121918063
hgdprs121918063
ensemblrs121918063
gopubmedrs121918063
geneviewrs121918063
scholarrs121918063
googlers121918063
pharmgkbrs121918063
gwascentralrs121918063
openSNPrs121918063
23andMers121918063
23andMe allrs121918063
SNP Nexus

SNPshotrs121918063
SNPdbers121918063
MSV3drs121918063
GWAS Ctlgrs121918063
Max Magnitude0
OMIM613521
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121918063(G;G)
Alt rs121918063(G;G)
Reference rs121918063(T;T)
Significance Pathogenic
Disease Familial porphyria cutanea tarda
Variation info
Gene UROD
CLNDBN Familial porphyria cutanea tarda
Reversed 0
HGVS NC_000001.10:g.45479600T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000091.3,