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rs10050257

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs10050257(G;G)
Make rs10050257(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154594243
is asnp
is mentioned by
dbSNPrs10050257
ebirs10050257
HLIrs10050257
Exacrs10050257
Varsomers10050257
Maprs10050257
PheGenIrs10050257
hapmaprs10050257
1000 genomesrs10050257
hgdprs10050257
ensemblrs10050257
gopubmedrs10050257
geneviewrs10050257
scholarrs10050257
googlers10050257
pharmgkbrs10050257
gwascentralrs10050257
openSNPrs10050257
23andMers10050257
23andMe allrs10050257
SNP Nexus

SNPshotrs10050257
SNPdbers10050257
MSV3drs10050257
GWAS Ctlgrs10050257
GMAF0.02342
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 20978265OA-icon.png] Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate gene Association Resource (CARe)