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rs398123125

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123125(G;T)
Make rs398123125(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position78885755
GeneARSB
is asnp
is mentioned by
dbSNPrs398123125
ebirs398123125
HLIrs398123125
Exacrs398123125
Varsomers398123125
Maprs398123125
PheGenIrs398123125
hapmaprs398123125
1000 genomesrs398123125
hgdprs398123125
ensemblrs398123125
gopubmedrs398123125
geneviewrs398123125
scholarrs398123125
googlers398123125
pharmgkbrs398123125
gwascentralrs398123125
openSNPrs398123125
23andMers398123125
23andMe allrs398123125
SNP Nexus

SNPshotrs398123125
SNPdbers398123125
MSV3drs398123125
GWAS Ctlgrs398123125
Max Magnitude0
ClinVar
Risk rs398123125(T;T)
Alt rs398123125(T;T)
Reference rs398123125(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ARSB
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.78181578C>A
CLNSRC HGMD
CLNACC RCV000078005.4,