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rs121918065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918065(A;A)
Make rs121918065(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position45014976
GeneUROD
is asnp
is mentioned by
dbSNPrs121918065
ebirs121918065
HLIrs121918065
Exacrs121918065
Varsomers121918065
Maprs121918065
PheGenIrs121918065
hapmaprs121918065
1000 genomesrs121918065
hgdprs121918065
ensemblrs121918065
gopubmedrs121918065
geneviewrs121918065
scholarrs121918065
googlers121918065
pharmgkbrs121918065
gwascentralrs121918065
openSNPrs121918065
23andMers121918065
23andMe allrs121918065
SNP Nexus

SNPshotrs121918065
SNPdbers121918065
MSV3drs121918065
GWAS Ctlgrs121918065
Max Magnitude0
OMIM613521
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121918065(A;A)
Alt rs121918065(A;A)
Reference rs121918065(C;C)
Significance Pathogenic
Disease Familial porphyria cutanea tarda
Variation info
Gene UROD
CLNDBN Familial porphyria cutanea tarda
Reversed 0
HGVS NC_000001.10:g.45480648C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000093.3,