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rs398123698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123698(A;A)
Make rs398123698(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position20348252
GeneUMOD
is asnp
is mentioned by
dbSNPrs398123698
ebirs398123698
HLIrs398123698
Exacrs398123698
Varsomers398123698
Maprs398123698
PheGenIrs398123698
hapmaprs398123698
1000 genomesrs398123698
hgdprs398123698
ensemblrs398123698
gopubmedrs398123698
geneviewrs398123698
scholarrs398123698
googlers398123698
pharmgkbrs398123698
gwascentralrs398123698
openSNPrs398123698
23andMers398123698
23andMe allrs398123698
SNP Nexus

SNPshotrs398123698
SNPdbers398123698
MSV3drs398123698
GWAS Ctlgrs398123698
Max Magnitude0
ClinVar
Risk rs398123698(A;A)
Alt rs398123698(A;A)
Reference rs398123698(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene UMOD
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.20359574C>T
CLNSRC HGMD
CLNACC RCV000080096.4,