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rs10521232

From SNPedia

Orientationplus
Stabilizedplus
Make rs10521232(C;C)
Make rs10521232(C;T)
Make rs10521232(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position13636487
is asnp
is mentioned by
dbSNPrs10521232
ebirs10521232
HLIrs10521232
Exacrs10521232
Varsomers10521232
Maprs10521232
PheGenIrs10521232
hapmaprs10521232
1000 genomesrs10521232
hgdprs10521232
ensemblrs10521232
gopubmedrs10521232
geneviewrs10521232
scholarrs10521232
googlers10521232
pharmgkbrs10521232
gwascentralrs10521232
openSNPrs10521232
23andMers10521232
23andMe allrs10521232
SNP Nexus

SNPshotrs10521232
SNPdbers10521232
MSV3drs10521232
GWAS Ctlgrs10521232
GMAF0.2952
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 0.0000039999999999999998
Odds Ratio NR NR


GET Evidence
rs10521232
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.383333
summary