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rs17172199

From SNPedia

Orientationplus
Stabilizedplus
Make rs17172199(A;A)
Make rs17172199(A;C)
Make rs17172199(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position43337677
GeneHECW1
is asnp
is mentioned by
dbSNPrs17172199
ebirs17172199
HLIrs17172199
Exacrs17172199
Varsomers17172199
Maprs17172199
PheGenIrs17172199
hapmaprs17172199
1000 genomesrs17172199
hgdprs17172199
ensemblrs17172199
gopubmedrs17172199
geneviewrs17172199
scholarrs17172199
googlers17172199
pharmgkbrs17172199
gwascentralrs17172199
openSNPrs17172199
23andMers17172199
23andMe allrs17172199
SNP Nexus

SNPshotrs17172199
SNPdbers17172199
MSV3drs17172199
GWAS Ctlgrs17172199
GMAF0.04086
Max Magnitude
GWAS snp
PMID [PMID 23535033OA-icon.png]
Trait Alzheimer's disease (cognitive decline)
Title Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
Risk Allele
P-val 1E-6
Odds Ratio .28 unit decrease