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rs1060499657

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499657(A;G)
Make rs1060499657(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position20348714
GeneUMOD
is asnp
is mentioned by
dbSNPrs1060499657
dbSNP (old)rs1060499657
ClinGenrs1060499657
ebirs1060499657
HLIrs1060499657
Exacrs1060499657
Gnomadrs1060499657
Varsomers1060499657
Maprs1060499657
PheGenIrs1060499657
Biobankrs1060499657
1000 genomesrs1060499657
hgdprs1060499657
ensemblrs1060499657
gopubmedrs1060499657
geneviewrs1060499657
scholarrs1060499657
googlers1060499657
pharmgkbrs1060499657
gwascentralrs1060499657
openSNPrs1060499657
23andMers1060499657
23andMe allrs1060499657
SNPshotrs1060499657
SNPdbers1060499657
MSV3drs1060499657
GWAS Ctlgrs1060499657
Max Magnitude0
ClinVar
Risk rs1060499657(G;G)
Alt rs1060499657(G;G)
Reference Rs1060499657(A;A)
Significance Probable-Pathogenic
Disease Familial juvenile gout
Variation info
Gene UMOD
CLNDBN Familial juvenile gout
Reversed 1
HGVS NC_000016.9:g.20360036T>C
CLNSRC
CLNACC RCV000449501.1,