Rs118203943

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Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118203943(A;G)
Make rs118203943(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position78964477
GeneARSB
is asnp
is mentioned by
dbSNPrs118203943
Exacrs118203943
PheGenIrs118203943
nextbiors118203943
hapmaprs118203943
1000 genomesrs118203943
hgdprs118203943
ensemblrs118203943
gopubmedrs118203943
geneviewrs118203943
scholarrs118203943
googlers118203943
pharmgkbrs118203943
gwascentralrs118203943
openSNPrs118203943
23andMers118203943
23andMe allrs118203943
SNP Nexus

SNPshotrs118203943
SNPdbers118203943
MSV3drs118203943
OMIM611542
Desc
Variant0009
Relatedalso
ClinVar
Risk rs118203943(G;G)
Alt rs118203943(G;G)
Reference rs118203943(A;A)
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.78260300T>C
CLNSRC Emory University OMIM Allelic Variant
CLNACC RCV000000933.2, RCV000078003.1,