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rs61754386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61754386(A;T)
Make rs61754386(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position89227897
GeneLOC107984363, TYR
is asnp
is mentioned by
dbSNPrs61754386
dbSNP (classic)rs61754386
ClinGenrs61754386
ebirs61754386
HLIrs61754386
Exacrs61754386
Gnomadrs61754386
Varsomers61754386
LitVarrs61754386
Maprs61754386
PheGenIrs61754386
Biobankrs61754386
1000 genomesrs61754386
hgdprs61754386
ensemblrs61754386
geneviewrs61754386
scholarrs61754386
googlers61754386
pharmgkbrs61754386
gwascentralrs61754386
openSNPrs61754386
23andMers61754386
SNPshotrs61754386
SNPdbers61754386
MSV3drs61754386
GWAS Ctlgrs61754386
Max Magnitude0
ClinVar
Risk rs61754386(T;T)
Alt rs61754386(T;T)
Reference Rs61754386(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TYR
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.88961065A>T
CLNSRC UniProtKB (protein)
CLNACC RCV000085896.1,