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rs4776472

From SNPedia

Orientationplus
Stabilizedplus
Make rs4776472(A;A)
Make rs4776472(A;G)
Make rs4776472(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position69714534
is asnp
is mentioned by
dbSNPrs4776472
ebirs4776472
HLIrs4776472
Exacrs4776472
Varsomers4776472
Maprs4776472
PheGenIrs4776472
hapmaprs4776472
1000 genomesrs4776472
hgdprs4776472
ensemblrs4776472
gopubmedrs4776472
geneviewrs4776472
scholarrs4776472
googlers4776472
pharmgkbrs4776472
gwascentralrs4776472
openSNPrs4776472
23andMers4776472
23andMe allrs4776472
SNP Nexus

SNPshotrs4776472
SNPdbers4776472
MSV3drs4776472
GWAS Ctlgrs4776472
GMAF0.3269
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs4776472
PubMedID [PMID 17903304OA-icon.png]
Condition Atrial fibrillation
Gene KIAA1598
Risk Allele
pValue 8.00E-006
OR NA
95% CI



GET Evidence
rs4776472
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary