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rs1064796028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTC;TTC) 0 common in clinvar
Chromosome11
Position89178759
GeneLOC107984363, TYR
is asnp
is mentioned by
dbSNPrs1064796028
dbSNP (old)rs1064796028
ClinGenrs1064796028
ebirs1064796028
HLIrs1064796028
Exacrs1064796028
Gnomadrs1064796028
Varsomers1064796028
Maprs1064796028
PheGenIrs1064796028
Biobankrs1064796028
1000 genomesrs1064796028
hgdprs1064796028
ensemblrs1064796028
gopubmedrs1064796028
geneviewrs1064796028
scholarrs1064796028
googlers1064796028
pharmgkbrs1064796028
gwascentralrs1064796028
openSNPrs1064796028
23andMers1064796028
23andMe allrs1064796028
SNPshotrs1064796028
SNPdbers1064796028
MSV3drs1064796028
GWAS Ctlgrs1064796028
Max Magnitude0
ClinVar
Risk rs1064796028(-;-)
Alt rs1064796028(-;-)
Reference Rs1064796028(TTC;TTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYR
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.88911927_88911929delTCT
CLNSRC
CLNACC RCV000478390.1,