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rs398123258

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123258(-;-)
Make rs398123258(-;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position1004083
GeneIDUA
is asnp
is mentioned by
dbSNPrs398123258
ebirs398123258
HLIrs398123258
Exacrs398123258
Varsomers398123258
Maprs398123258
PheGenIrs398123258
hapmaprs398123258
1000 genomesrs398123258
hgdprs398123258
ensemblrs398123258
gopubmedrs398123258
geneviewrs398123258
scholarrs398123258
googlers398123258
pharmgkbrs398123258
gwascentralrs398123258
openSNPrs398123258
23andMers398123258
23andMe allrs398123258
SNP Nexus

SNPshotrs398123258
SNPdbers398123258
MSV3drs398123258
GWAS Ctlgrs398123258
Max Magnitude0
ClinVar
Risk rs398123258(;)
Alt rs398123258(;)
Reference rs398123258(C;C)
Significance Pathogenic
Disease not provided Hurler syndrome
Variation info
Gene IDUA
CLNDBN not provided Hurler syndrome
Reversed 0
HGVS NC_000004.11:g.997871delC
CLNSRC ClinVar
CLNACC RCV000078385.3, RCV000174452.1,