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rs1448817

From SNPedia

Orientationplus
Make rs1448817(A;A)
Make rs1448817(A;G)
Make rs1448817(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position110719897
is asnp
is mentioned by
dbSNPrs1448817
ebirs1448817
HLIrs1448817
Exacrs1448817
Varsomers1448817
Maprs1448817
PheGenIrs1448817
hapmaprs1448817
1000 genomesrs1448817
hgdprs1448817
ensemblrs1448817
gopubmedrs1448817
geneviewrs1448817
scholarrs1448817
googlers1448817
pharmgkbrs1448817
gwascentralrs1448817
openSNPrs1448817
23andMers1448817
23andMe allrs1448817
SNP Nexus

SNPshotrs1448817
SNPdbers1448817
MSV3drs1448817
GWAS Ctlgrs1448817
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 26497660] Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF)