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rs2935776

From SNPedia

Orientationminus
Stabilizedminus
Make rs2935776(C;C)
Make rs2935776(C;T)
Make rs2935776(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position108617674
is asnp
is mentioned by
dbSNPrs2935776
ebirs2935776
HLIrs2935776
Exacrs2935776
Varsomers2935776
Maprs2935776
PheGenIrs2935776
hapmaprs2935776
1000 genomesrs2935776
hgdprs2935776
ensemblrs2935776
gopubmedrs2935776
geneviewrs2935776
scholarrs2935776
googlers2935776
pharmgkbrs2935776
gwascentralrs2935776
openSNPrs2935776
23andMers2935776
23andMe allrs2935776
SNP Nexus

SNPshotrs2935776
SNPdbers2935776
MSV3drs2935776
GWAS Ctlgrs2935776
GMAF0.2424
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 6E-7
Odds Ratio None None