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rs10767971

From SNPedia

Orientationplus
Stabilizedplus
Make rs10767971(C;C)
Make rs10767971(C;T)
Make rs10767971(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position32874118
is asnp
is mentioned by
dbSNPrs10767971
ebirs10767971
HLIrs10767971
Exacrs10767971
Varsomers10767971
Maprs10767971
PheGenIrs10767971
hapmaprs10767971
1000 genomesrs10767971
hgdprs10767971
ensemblrs10767971
gopubmedrs10767971
geneviewrs10767971
scholarrs10767971
googlers10767971
pharmgkbrs10767971
gwascentralrs10767971
openSNPrs10767971
23andMers10767971
23andMe allrs10767971
SNP Nexus

SNPshotrs10767971
SNPdbers10767971
MSV3drs10767971
GWAS Ctlgrs10767971
GMAF0.365
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19772629OA-icon.png] Genomewide association study for onset age in Parkinson disease


GET Evidence
rs10767971
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.601562
summary