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rs12899449

From SNPedia

Orientationplus
Stabilizedplus
Make rs12899449(A;A)
Make rs12899449(A;G)
Make rs12899449(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position38703290
is asnp
is mentioned by
dbSNPrs12899449
ebirs12899449
HLIrs12899449
Exacrs12899449
Varsomers12899449
Maprs12899449
PheGenIrs12899449
hapmaprs12899449
1000 genomesrs12899449
hgdprs12899449
ensemblrs12899449
gopubmedrs12899449
geneviewrs12899449
scholarrs12899449
googlers12899449
pharmgkbrs12899449
gwascentralrs12899449
openSNPrs12899449
23andMers12899449
23andMe allrs12899449
SNP Nexus

SNPshotrs12899449
SNPdbers12899449
MSV3drs12899449
GWAS Ctlgrs12899449
GMAF0.1731
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs12899449
PubMedID [PMID 18711365OA-icon.png]
Condition Bipolar disorder
Gene C15orf53, RASGRP1
Risk Allele
pValue 4.00E-007
OR 1.2
95% CI



GET Evidence
rs12899449
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary