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rs7849530

From SNPedia

Orientationplus
Stabilizedplus
Make rs7849530(A;A)
Make rs7849530(A;G)
Make rs7849530(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position92165453
is asnp
is mentioned by
dbSNPrs7849530
dbSNP (classic)rs7849530
ClinGenrs7849530
ebirs7849530
HLIrs7849530
Exacrs7849530
Gnomadrs7849530
Varsomers7849530
LitVarrs7849530
Maprs7849530
PheGenIrs7849530
Biobankrs7849530
1000 genomesrs7849530
hgdprs7849530
ensemblrs7849530
geneviewrs7849530
scholarrs7849530
googlers7849530
pharmgkbrs7849530
gwascentralrs7849530
openSNPrs7849530
23andMers7849530
SNPshotrs7849530
SNPdbers7849530
MSV3drs7849530
GWAS Ctlgrs7849530
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 25140149OA-icon.png] Genetic variation modifies risk for neurodegeneration based on biomarker status