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rs10514688

From SNPedia

Orientationplus
Stabilizedplus
Make rs10514688(C;C)
Make rs10514688(C;T)
Make rs10514688(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position34921177
GeneLOC101928135
is asnp
is mentioned by
dbSNPrs10514688
ebirs10514688
HLIrs10514688
Exacrs10514688
Varsomers10514688
Maprs10514688
PheGenIrs10514688
hapmaprs10514688
1000 genomesrs10514688
hgdprs10514688
ensemblrs10514688
gopubmedrs10514688
geneviewrs10514688
scholarrs10514688
googlers10514688
pharmgkbrs10514688
gwascentralrs10514688
openSNPrs10514688
23andMers10514688
23andMe allrs10514688
SNP Nexus

SNPshotrs10514688
SNPdbers10514688
MSV3drs10514688
GWAS Ctlgrs10514688
GMAF0.1299
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903302OA-icon.png]
Trait Tonometry
Title Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
Risk Allele
P-val 0.0000060000000000000002
Odds Ratio NR NR


GET Evidence
rs10514688
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary