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rs886041370

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position80214206
GeneSGSH
is asnp
is mentioned by
dbSNPrs886041370
dbSNP (classic)rs886041370
ClinGenrs886041370
ebirs886041370
HLIrs886041370
Exacrs886041370
Gnomadrs886041370
Varsomers886041370
LitVarrs886041370
Maprs886041370
PheGenIrs886041370
Biobankrs886041370
1000 genomesrs886041370
hgdprs886041370
ensemblrs886041370
geneviewrs886041370
scholarrs886041370
googlers886041370
pharmgkbrs886041370
gwascentralrs886041370
openSNPrs886041370
23andMers886041370
SNPshotrs886041370
SNPdbers886041370
MSV3drs886041370
GWAS Ctlgrs886041370
Max Magnitude0
ClinVar
Risk rs886041370(A;A)
Alt rs886041370(A;A)
Reference Rs886041370(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SGSH
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.78188005C>T
CLNSRC
CLNACC RCV000345601.1,