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rs121917774

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917774(G;T)
Make rs121917774(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position20348484
GeneUMOD
is asnp
is mentioned by
dbSNPrs121917774
ebirs121917774
HLIrs121917774
Exacrs121917774
Varsomers121917774
Maprs121917774
PheGenIrs121917774
hapmaprs121917774
1000 genomesrs121917774
hgdprs121917774
ensemblrs121917774
gopubmedrs121917774
geneviewrs121917774
scholarrs121917774
googlers121917774
pharmgkbrs121917774
gwascentralrs121917774
openSNPrs121917774
23andMers121917774
23andMe allrs121917774
SNP Nexus

SNPshotrs121917774
SNPdbers121917774
MSV3drs121917774
GWAS Ctlgrs121917774
Max Magnitude0
OMIM191845
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121917774(T;T)
Alt rs121917774(T;T)
Reference rs121917774(G;G)
Significance Pathogenic
Disease Familial juvenile gout
Variation info
Gene UMOD
CLNDBN Familial juvenile gout
Reversed 1
HGVS NC_000016.9:g.20359806C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013051.16,