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rs7506045

From SNPedia

Orientationplus
Stabilizedplus
Make rs7506045(C;C)
Make rs7506045(C;T)
Make rs7506045(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position11987273
GeneIMPA2
is asnp
is mentioned by
dbSNPrs7506045
ebirs7506045
HLIrs7506045
Exacrs7506045
Varsomers7506045
Maprs7506045
PheGenIrs7506045
hapmaprs7506045
1000 genomesrs7506045
hgdprs7506045
ensemblrs7506045
gopubmedrs7506045
geneviewrs7506045
scholarrs7506045
googlers7506045
pharmgkbrs7506045
gwascentralrs7506045
openSNPrs7506045
23andMers7506045
23andMe allrs7506045
SNP Nexus

SNPshotrs7506045
SNPdbers7506045
MSV3drs7506045
GWAS Ctlgrs7506045
GMAF0.1556
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs7506045
PubMedID [PMID 17434096OA-icon.png]
Condition Stroke
Gene IMPA2
Risk Allele
pValue 7.00E-007
OR 5.39
95% CI 2.77-10.5


[PMID 19647252] KCNK17 genetic variants in ischemic stroke



GET Evidence
rs7506045
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.15625
summary