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rs1064795109

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position80210532
GeneSGSH
is asnp
is mentioned by
dbSNPrs1064795109
dbSNP (old)rs1064795109
ClinGenrs1064795109
ebirs1064795109
HLIrs1064795109
Exacrs1064795109
Gnomadrs1064795109
Varsomers1064795109
LitVarrs1064795109
Maprs1064795109
PheGenIrs1064795109
Biobankrs1064795109
1000 genomesrs1064795109
hgdprs1064795109
ensemblrs1064795109
gopubmedrs1064795109
geneviewrs1064795109
scholarrs1064795109
googlers1064795109
pharmgkbrs1064795109
gwascentralrs1064795109
openSNPrs1064795109
23andMers1064795109
23andMe allrs1064795109
SNPshotrs1064795109
SNPdbers1064795109
MSV3drs1064795109
GWAS Ctlgrs1064795109
Max Magnitude0
ClinVar
Risk rs1064795109(A;A)
Alt rs1064795109(A;A)
Reference Rs1064795109(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SGSH
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.78184331C>T
CLNSRC
CLNACC RCV000485142.1,