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rs17265593

From SNPedia

Orientationplus
Stabilizedplus
Make rs17265593(C;C)
Make rs17265593(C;T)
Make rs17265593(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position37580319
is asnp
is mentioned by
dbSNPrs17265593
dbSNP (classic)rs17265593
ClinGenrs17265593
ebirs17265593
HLIrs17265593
Exacrs17265593
Gnomadrs17265593
Varsomers17265593
LitVarrs17265593
Maprs17265593
PheGenIrs17265593
Biobankrs17265593
1000 genomesrs17265593
hgdprs17265593
ensemblrs17265593
geneviewrs17265593
scholarrs17265593
googlers17265593
pharmgkbrs17265593
gwascentralrs17265593
openSNPrs17265593
23andMers17265593
SNPshotrs17265593
SNPdbers17265593
MSV3drs17265593
GWAS Ctlgrs17265593
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 28323831OA-icon.png] Alzheimer's disease polygenic hazard score