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rs1379659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs1379659(A;G)
Make rs1379659(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position20619060
GeneSLIT2
is asnp
is mentioned by
dbSNPrs1379659
ebirs1379659
HLIrs1379659
Exacrs1379659
Varsomers1379659
Maprs1379659
PheGenIrs1379659
hapmaprs1379659
1000 genomesrs1379659
hgdprs1379659
ensemblrs1379659
gopubmedrs1379659
geneviewrs1379659
scholarrs1379659
googlers1379659
pharmgkbrs1379659
gwascentralrs1379659
openSNPrs1379659
23andMers1379659
23andMe allrs1379659
SNP Nexus

SNPshotrs1379659
SNPdbers1379659
MSV3drs1379659
GWAS Ctlgrs1379659
GMAF0.1345
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 17903301OA-icon.png] Left ventricle diastolic dimension, rs1379659 (SLIT2, p = 1.17*10(-7))
GWAS
SNP rs1379659
PubMedID [PMID 17903301OA-icon.png]
Condition Echocardiographic traits
Gene SLIT2
Risk Allele
pValue 1.00E-007
OR NA
95% CI



GET Evidence
rs1379659
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.855921
summary