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rs121917771

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917771(A;A)
Make rs121917771(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position20348537
GeneUMOD
is asnp
is mentioned by
dbSNPrs121917771
ebirs121917771
HLIrs121917771
Exacrs121917771
Varsomers121917771
Maprs121917771
PheGenIrs121917771
hapmaprs121917771
1000 genomesrs121917771
hgdprs121917771
ensemblrs121917771
gopubmedrs121917771
geneviewrs121917771
scholarrs121917771
googlers121917771
pharmgkbrs121917771
gwascentralrs121917771
openSNPrs121917771
23andMers121917771
23andMe allrs121917771
SNP Nexus

SNPshotrs121917771
SNPdbers121917771
MSV3drs121917771
GWAS Ctlgrs121917771
Max Magnitude0
OMIM191845
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121917771(A;A)
Alt rs121917771(A;A)
Reference rs121917771(G;G)
Significance Pathogenic
Disease Familial juvenile gout
Variation info
Gene UMOD
CLNDBN Familial juvenile gout
Reversed 1
HGVS NC_000016.9:g.20359859C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013048.23,