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rs1943816

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs1943816(C;C)
Make rs1943816(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position73391387
is asnp
is mentioned by
dbSNPrs1943816
dbSNP (classic)rs1943816
ClinGenrs1943816
ebirs1943816
HLIrs1943816
Exacrs1943816
Gnomadrs1943816
Varsomers1943816
LitVarrs1943816
Maprs1943816
PheGenIrs1943816
Biobankrs1943816
1000 genomesrs1943816
hgdprs1943816
ensemblrs1943816
geneviewrs1943816
scholarrs1943816
googlers1943816
pharmgkbrs1943816
gwascentralrs1943816
openSNPrs1943816
23andMers1943816
SNPshotrs1943816
SNPdbers1943816
MSV3drs1943816
GWAS Ctlgrs1943816
GMAF0.1942
Max Magnitude0
? (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 1E-7
Odds Ratio None None