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rs17006206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17006206(A;G)
Make rs17006206(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position27684606
GeneSLC4A1AP
is asnp
is mentioned by
dbSNPrs17006206
ebirs17006206
HLIrs17006206
Exacrs17006206
Varsomers17006206
Maprs17006206
PheGenIrs17006206
hapmaprs17006206
1000 genomesrs17006206
hgdprs17006206
ensemblrs17006206
gopubmedrs17006206
geneviewrs17006206
scholarrs17006206
googlers17006206
pharmgkbrs17006206
gwascentralrs17006206
openSNPrs17006206
23andMers17006206
23andMe allrs17006206
SNP Nexus

SNPshotrs17006206
SNPdbers17006206
MSV3drs17006206
GWAS Ctlgrs17006206
GMAF0.0202
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22159054OA-icon.png]
Trait
Title A comprehensive genetic association study of Alzheimer disease in African Americans.
Risk Allele G
P-val 0.000002
Odds Ratio 2.0500 None