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rs511154

From SNPedia

Orientationplus
Stabilizedplus
Make rs511154(A;A)
Make rs511154(A;G)
Make rs511154(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position136232079
is asnp
is mentioned by
dbSNPrs511154
ebirs511154
HLIrs511154
Exacrs511154
Varsomers511154
Maprs511154
PheGenIrs511154
hapmaprs511154
1000 genomesrs511154
hgdprs511154
ensemblrs511154
gopubmedrs511154
geneviewrs511154
scholarrs511154
googlers511154
pharmgkbrs511154
gwascentralrs511154
openSNPrs511154
23andMers511154
23andMe allrs511154
SNP Nexus

SNPshotrs511154
SNPdbers511154
MSV3drs511154
GWAS Ctlgrs511154
GMAF0.2319
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20031576OA-icon.png] Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts


GET Evidence
rs511154
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.726562
summary