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rs9574199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9574199(A;A)
Make rs9574199(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position78234779
GeneRNF219-AS1
is asnp
is mentioned by
dbSNPrs9574199
dbSNP (classic)rs9574199
ClinGenrs9574199
ebirs9574199
HLIrs9574199
Exacrs9574199
Gnomadrs9574199
Varsomers9574199
LitVarrs9574199
Maprs9574199
PheGenIrs9574199
Biobankrs9574199
1000 genomesrs9574199
hgdprs9574199
ensemblrs9574199
geneviewrs9574199
scholarrs9574199
googlers9574199
pharmgkbrs9574199
gwascentralrs9574199
openSNPrs9574199
23andMers9574199
SNPshotrs9574199
SNPdbers9574199
MSV3drs9574199
GWAS Ctlgrs9574199
GMAF0.4848
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 21116278OA-icon.png]
Trait
Title Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
Risk Allele
P-val 0.000007
Odds Ratio 0.0041 [NR] unit increase (interaction)