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rs121917768

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917768(A;A)
Make rs121917768(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position20349071
GeneUMOD
is asnp
is mentioned by
dbSNPrs121917768
ebirs121917768
HLIrs121917768
Exacrs121917768
Varsomers121917768
Maprs121917768
PheGenIrs121917768
hapmaprs121917768
1000 genomesrs121917768
hgdprs121917768
ensemblrs121917768
gopubmedrs121917768
geneviewrs121917768
scholarrs121917768
googlers121917768
pharmgkbrs121917768
gwascentralrs121917768
openSNPrs121917768
23andMers121917768
23andMe allrs121917768
SNP Nexus

SNPshotrs121917768
SNPdbers121917768
MSV3drs121917768
GWAS Ctlgrs121917768
Max Magnitude0
OMIM191845
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121917768(A;A)
Alt rs121917768(A;A)
Reference rs121917768(G;G)
Significance Pathogenic
Disease Familial juvenile gout
Variation info
Gene UMOD
CLNDBN Familial juvenile gout
Reversed 1
HGVS NC_000016.9:g.20360393C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013045.23,