Have questions? Visit https://www.reddit.com/r/SNPedia

rs366676

From SNPedia

Orientationminus
Stabilizedminus
Make rs366676(C;C)
Make rs366676(C;T)
Make rs366676(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position88008048
is asnp
is mentioned by
dbSNPrs366676
ebirs366676
HLIrs366676
Exacrs366676
Varsomers366676
Maprs366676
PheGenIrs366676
hapmaprs366676
1000 genomesrs366676
hgdprs366676
ensemblrs366676
gopubmedrs366676
geneviewrs366676
scholarrs366676
googlers366676
pharmgkbrs366676
gwascentralrs366676
openSNPrs366676
23andMers366676
23andMe allrs366676
SNP Nexus

SNPshotrs366676
SNPdbers366676
MSV3drs366676
GWAS Ctlgrs366676
GMAF0.4587
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs366676
PubMedID [PMID 17903301OA-icon.png]
Condition Echocardiographic traits
Gene SPACA1
Risk Allele
pValue 2.00E-006
OR NA
95% CI



GET Evidence
rs366676
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.445312
summary