Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779401

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779401(A;G)
Make rs587779401(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position1004305
GeneIDUA, LOC105374342
is asnp
is mentioned by
dbSNPrs587779401
ebirs587779401
HLIrs587779401
Exacrs587779401
Varsomers587779401
Maprs587779401
PheGenIrs587779401
hapmaprs587779401
1000 genomesrs587779401
hgdprs587779401
ensemblrs587779401
gopubmedrs587779401
geneviewrs587779401
scholarrs587779401
googlers587779401
pharmgkbrs587779401
gwascentralrs587779401
openSNPrs587779401
23andMers587779401
23andMe allrs587779401
SNP Nexus

SNPshotrs587779401
SNPdbers587779401
MSV3drs587779401
GWAS Ctlgrs587779401
Max Magnitude0
ClinVar
Risk rs587779401(G;G)
Alt rs587779401(G;G)
Reference rs587779401(A;A)
Significance Pathogenic
Disease Hurler syndrome
Variation info
Gene IDUA
CLNDBN Hurler syndrome
Reversed 0
HGVS NC_000004.11:g.998093A>G
CLNSRC
CLNACC RCV000087088.1,