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rs7577851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7577851(C;T)
Make rs7577851(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position69496578
GeneAAK1
is asnp
is mentioned by
dbSNPrs7577851
ebirs7577851
HLIrs7577851
Exacrs7577851
Varsomers7577851
Maprs7577851
PheGenIrs7577851
hapmaprs7577851
1000 genomesrs7577851
hgdprs7577851
ensemblrs7577851
gopubmedrs7577851
geneviewrs7577851
scholarrs7577851
googlers7577851
pharmgkbrs7577851
gwascentralrs7577851
openSNPrs7577851
23andMers7577851
23andMe allrs7577851
SNP Nexus

SNPshotrs7577851
SNPdbers7577851
MSV3drs7577851
GWAS Ctlgrs7577851
GMAF0.3306
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19772629OA-icon.png] Genomewide association study for onset age in Parkinson disease


GET Evidence
rs7577851
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.367188
summary