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rs540911439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs540911439(C;T)
Make rs540911439(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position89191358
GeneLOC107984363, TYR
is asnp
is mentioned by
dbSNPrs540911439
dbSNP (classic)rs540911439
ClinGenrs540911439
ebirs540911439
HLIrs540911439
Exacrs540911439
Gnomadrs540911439
Varsomers540911439
LitVarrs540911439
Maprs540911439
PheGenIrs540911439
Biobankrs540911439
1000 genomesrs540911439
hgdprs540911439
ensemblrs540911439
geneviewrs540911439
scholarrs540911439
googlers540911439
pharmgkbrs540911439
gwascentralrs540911439
openSNPrs540911439
23andMers540911439
SNPshotrs540911439
SNPdbers540911439
MSV3drs540911439
GWAS Ctlgrs540911439
Max Magnitude0
ClinVar
Risk rs540911439(T;T)
Alt rs540911439(T;T)
Reference Rs540911439(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TYR
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.88924526C>T
CLNSRC
CLNACC RCV000429411.1,