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rs1727638

From SNPedia

Orientationplus
Stabilizedplus
Make rs1727638(A;A)
Make rs1727638(A;G)
Make rs1727638(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position71429869
GeneLINC01626
is asnp
is mentioned by
dbSNPrs1727638
dbSNP (classic)rs1727638
ClinGenrs1727638
ebirs1727638
HLIrs1727638
Exacrs1727638
Gnomadrs1727638
Varsomers1727638
LitVarrs1727638
Maprs1727638
PheGenIrs1727638
Biobankrs1727638
1000 genomesrs1727638
hgdprs1727638
ensemblrs1727638
geneviewrs1727638
scholarrs1727638
googlers1727638
pharmgkbrs1727638
gwascentralrs1727638
openSNPrs1727638
23andMers1727638
SNPshotrs1727638
SNPdbers1727638
MSV3drs1727638
GWAS Ctlgrs1727638
GMAF0.4545
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20932310OA-icon.png]
Trait
Title Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study
Risk Allele A
P-val 0.000001
Odds Ratio None None