Rs118203942

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203942(A;A)
Make rs118203942(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position78984965
GeneARSB
is asnp
is mentioned by
dbSNPrs118203942
Exacrs118203942
PheGenIrs118203942
nextbiors118203942
hapmaprs118203942
1000 genomesrs118203942
hgdprs118203942
ensemblrs118203942
gopubmedrs118203942
geneviewrs118203942
scholarrs118203942
googlers118203942
pharmgkbrs118203942
gwascentralrs118203942
openSNPrs118203942
23andMers118203942
23andMe allrs118203942
SNP Nexus

SNPshotrs118203942
SNPdbers118203942
MSV3drs118203942
OMIM611542
Desc
Variant0008
Relatedalso
ClinVar
Risk rs118203942(A;A)
Alt rs118203942(A;A)
Reference rs118203942(G;G)
Significance Pathogenic
Disease Mucopolysaccharidosis type VI not provided
Variation info
Gene ARSB
CLNDBN Mucopolysaccharidosis type VI not provided
Reversed 1
HGVS NC_000005.9:g.78280788C>T
CLNSRC Emory University OMIM Allelic Variant
CLNACC RCV000000932.2, RCV000078002.1,