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rs1991867

From SNPedia

Orientationminus
Stabilizedminus
Make rs1991867(A;A)
Make rs1991867(A;G)
Make rs1991867(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position82485623
is asnp
is mentioned by
dbSNPrs1991867
ebirs1991867
HLIrs1991867
Exacrs1991867
Varsomers1991867
Maprs1991867
PheGenIrs1991867
hapmaprs1991867
1000 genomesrs1991867
hgdprs1991867
ensemblrs1991867
gopubmedrs1991867
geneviewrs1991867
scholarrs1991867
googlers1991867
pharmgkbrs1991867
gwascentralrs1991867
openSNPrs1991867
23andMers1991867
23andMe allrs1991867
SNP Nexus

SNPshotrs1991867
SNPdbers1991867
MSV3drs1991867
GWAS Ctlgrs1991867
GMAF0.2185
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21502573OA-icon.png]
Trait
Title Genetic predictors of fibrin D-dimer levels in healthy adults.
Risk Allele C
P-val 0.000004
Odds Ratio 0.0440 [NR] % decrease
GWAS snp
PMID [PMID 24736177OA-icon.png]
Trait White matter microstructure (global fractional anisotropy)
Title Common genetic variants and gene expression associated with white matter microstructure in the human brain.
Risk Allele
P-val 2E-9
Odds Ratio NR NR