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rs11934801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11934801(C;C)
Make rs11934801(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position1002767
GeneIDUA
is asnp
is mentioned by
dbSNPrs11934801
ebirs11934801
HLIrs11934801
Exacrs11934801
Varsomers11934801
Maprs11934801
PheGenIrs11934801
hapmaprs11934801
1000 genomesrs11934801
hgdprs11934801
ensemblrs11934801
gopubmedrs11934801
geneviewrs11934801
scholarrs11934801
googlers11934801
pharmgkbrs11934801
gwascentralrs11934801
openSNPrs11934801
23andMers11934801
23andMe allrs11934801
SNP Nexus

SNPshotrs11934801
SNPdbers11934801
MSV3drs11934801
GWAS Ctlgrs11934801
GMAF0.01653
Max Magnitude0
OMIM252800
DescHURLER SYNDROME
Variant0005
Relatedalso


ClinVar
Risk rs11934801(C;C)
Alt rs11934801(C;C)
Reference rs11934801(G;G)
Significance Other
Disease Hurler syndrome not specified
Variation info
Gene IDUA
CLNDBN Hurler syndrome not specified
Reversed 0
HGVS NC_000004.11:g.996555G>C
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000012686.22, RCV000078375.4,