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rs398122388

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122388(C;C)
Make rs398122388(C;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position20348558
GeneUMOD
is asnp
is mentioned by
dbSNPrs398122388
ebirs398122388
HLIrs398122388
Exacrs398122388
Varsomers398122388
Maprs398122388
PheGenIrs398122388
hapmaprs398122388
1000 genomesrs398122388
hgdprs398122388
ensemblrs398122388
gopubmedrs398122388
geneviewrs398122388
scholarrs398122388
googlers398122388
pharmgkbrs398122388
gwascentralrs398122388
openSNPrs398122388
23andMers398122388
23andMe allrs398122388
SNP Nexus

SNPshotrs398122388
SNPdbers398122388
MSV3drs398122388
GWAS Ctlgrs398122388
Max Magnitude0
ClinVar
Risk rs398122388(C;C)
Alt rs398122388(C;C)
Reference rs398122388(G;G)
Significance Pathogenic
Disease Familial juvenile gout
Variation info
Gene UMOD
CLNDBN Familial juvenile gout
Reversed 1
HGVS NC_000016.9:g.20359880C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000054814.22,