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rs1085307880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome8
Position43170690
GeneHGSNAT
is asnp
is mentioned by
dbSNPrs1085307880
dbSNP (old)rs1085307880
ClinGenrs1085307880
ebirs1085307880
HLIrs1085307880
Exacrs1085307880
Gnomadrs1085307880
Varsomers1085307880
LitVarrs1085307880
Maprs1085307880
PheGenIrs1085307880
Biobankrs1085307880
1000 genomesrs1085307880
hgdprs1085307880
ensemblrs1085307880
gopubmedrs1085307880
geneviewrs1085307880
scholarrs1085307880
googlers1085307880
pharmgkbrs1085307880
gwascentralrs1085307880
openSNPrs1085307880
23andMers1085307880
23andMe allrs1085307880
SNPshotrs1085307880
SNPdbers1085307880
MSV3drs1085307880
GWAS Ctlgrs1085307880
Max Magnitude0
ClinVar
Risk rs1085307880(-;-)
Alt rs1085307880(-;-)
Reference Rs1085307880(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene HGSNAT
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.43025833delA
CLNSRC
CLNACC RCV000489181.1,