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rs1829883

From SNPedia

Orientationplus
Stabilizedplus
Make rs1829883(C;C)
Make rs1829883(C;T)
Make rs1829883(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position99445399
is asnp
is mentioned by
dbSNPrs1829883
ebirs1829883
HLIrs1829883
Exacrs1829883
Varsomers1829883
Maprs1829883
PheGenIrs1829883
hapmaprs1829883
1000 genomesrs1829883
hgdprs1829883
ensemblrs1829883
gopubmedrs1829883
geneviewrs1829883
scholarrs1829883
googlers1829883
pharmgkbrs1829883
gwascentralrs1829883
openSNPrs1829883
23andMers1829883
23andMe allrs1829883
SNP Nexus

SNPshotrs1829883
SNPdbers1829883
MSV3drs1829883
GWAS Ctlgrs1829883
GMAF0.3871
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903294OA-icon.png]
Trait Hemostatic factors and hematological phenotypes
Title Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
Risk Allele
P-val 0.0000060000000000000002
Odds Ratio NR NR


GET Evidence
rs1829883
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.34375
summary