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rs10488172

From SNPedia

Orientationplus
Stabilizedplus
Make rs10488172(G;G)
Make rs10488172(G;T)
Make rs10488172(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position133650423
GeneEXOC4
is asnp
is mentioned by
dbSNPrs10488172
ebirs10488172
HLIrs10488172
Exacrs10488172
Varsomers10488172
Maprs10488172
PheGenIrs10488172
hapmaprs10488172
1000 genomesrs10488172
hgdprs10488172
ensemblrs10488172
gopubmedrs10488172
geneviewrs10488172
scholarrs10488172
googlers10488172
pharmgkbrs10488172
gwascentralrs10488172
openSNPrs10488172
23andMers10488172
23andMe allrs10488172
SNP Nexus

SNPshotrs10488172
SNPdbers10488172
MSV3drs10488172
GWAS Ctlgrs10488172
GMAF0.2819
Max Magnitude
? (G;G) (G;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 0.0000079999999999999996
Odds Ratio NR NR


[PMID 18559547OA-icon.png] Comparing genetic ancestry and self-described race in african americans born in the United States and in Africa.


[PMID 19107526OA-icon.png] Population admixture associated with disease prevalence in the Boston Puerto Rican health study.


GET Evidence
rs10488172
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary