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rs786200863

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs786200863(-;-)
Make rs786200863(-;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position65973676
GeneGUSB
is asnp
is mentioned by
dbSNPrs786200863
ebirs786200863
HLIrs786200863
Exacrs786200863
Varsomers786200863
Maprs786200863
PheGenIrs786200863
hapmaprs786200863
1000 genomesrs786200863
hgdprs786200863
ensemblrs786200863
gopubmedrs786200863
geneviewrs786200863
scholarrs786200863
googlers786200863
pharmgkbrs786200863
gwascentralrs786200863
openSNPrs786200863
23andMers786200863
23andMe allrs786200863
SNP Nexus

SNPshotrs786200863
SNPdbers786200863
MSV3drs786200863
GWAS Ctlgrs786200863
Max Magnitude0
ClinVar
Risk rs786200863(;)
Alt rs786200863(;)
Reference rs786200863(TC;TC)
Significance Pathogenic
Disease Mucopolysaccharidosis type VII
Variation info
Gene GUSB
CLNDBN Mucopolysaccharidosis type VII
Reversed 1
HGVS NC_000007.13:g.65438663_65438664delGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000000951.5,