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rs1064795343

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome11
Position89178477
GeneLOC107984363, TYR
is asnp
is mentioned by
dbSNPrs1064795343
dbSNP (old)rs1064795343
ClinGenrs1064795343
ebirs1064795343
HLIrs1064795343
Exacrs1064795343
Gnomadrs1064795343
Varsomers1064795343
LitVarrs1064795343
Maprs1064795343
PheGenIrs1064795343
Biobankrs1064795343
1000 genomesrs1064795343
hgdprs1064795343
ensemblrs1064795343
gopubmedrs1064795343
geneviewrs1064795343
scholarrs1064795343
googlers1064795343
pharmgkbrs1064795343
gwascentralrs1064795343
openSNPrs1064795343
23andMers1064795343
23andMe allrs1064795343
SNPshotrs1064795343
SNPdbers1064795343
MSV3drs1064795343
GWAS Ctlgrs1064795343
Max Magnitude0
ClinVar
Risk rs1064795343(C;C)
Alt rs1064795343(C;C)
Reference Rs1064795343(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYR
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.88911645T>C
CLNSRC
CLNACC RCV000486330.1,