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rs935334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs935334(C;T)
Make rs935334(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position76147335
is asnp
is mentioned by
dbSNPrs935334
ebirs935334
HLIrs935334
Exacrs935334
Varsomers935334
Maprs935334
PheGenIrs935334
hapmaprs935334
1000 genomesrs935334
hgdprs935334
ensemblrs935334
gopubmedrs935334
geneviewrs935334
scholarrs935334
googlers935334
pharmgkbrs935334
gwascentralrs935334
openSNPrs935334
23andMers935334
23andMe allrs935334
SNP Nexus

SNPshotrs935334
SNPdbers935334
MSV3drs935334
GWAS Ctlgrs935334
GMAF0.208
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs935334
PubMedID [PMID 17903302OA-icon.png]
Condition Blood pressure
Gene Intergenic
Risk Allele
pValue 3.00E-006
OR NA
95% CI

[PMID 17903302OA-icon.png] diastolic blood pressure



GET Evidence
rs935334
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.703125
summary