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rs1064794815

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position80210766
GeneSGSH
is asnp
is mentioned by
dbSNPrs1064794815
dbSNP (old)rs1064794815
ClinGenrs1064794815
ebirs1064794815
HLIrs1064794815
Exacrs1064794815
Gnomadrs1064794815
Varsomers1064794815
Maprs1064794815
PheGenIrs1064794815
Biobankrs1064794815
1000 genomesrs1064794815
hgdprs1064794815
ensemblrs1064794815
gopubmedrs1064794815
geneviewrs1064794815
scholarrs1064794815
googlers1064794815
pharmgkbrs1064794815
gwascentralrs1064794815
openSNPrs1064794815
23andMers1064794815
23andMe allrs1064794815
SNPshotrs1064794815
SNPdbers1064794815
MSV3drs1064794815
GWAS Ctlgrs1064794815
Max Magnitude0
ClinVar
Risk rs1064794815(A;A)
Alt rs1064794815(A;A)
Reference Rs1064794815(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SGSH
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.78184565C>T
CLNSRC
CLNACC RCV000478188.1,