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rs6574988

From SNPedia

Orientationplus
Stabilizedplus
Make rs6574988(C;C)
Make rs6574988(C;T)
Make rs6574988(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position88093648
is asnp
is mentioned by
dbSNPrs6574988
ebirs6574988
HLIrs6574988
Exacrs6574988
Varsomers6574988
Maprs6574988
PheGenIrs6574988
hapmaprs6574988
1000 genomesrs6574988
hgdprs6574988
ensemblrs6574988
gopubmedrs6574988
geneviewrs6574988
scholarrs6574988
googlers6574988
pharmgkbrs6574988
gwascentralrs6574988
openSNPrs6574988
23andMers6574988
23andMe allrs6574988
SNP Nexus

SNPshotrs6574988
SNPdbers6574988
MSV3drs6574988
GWAS Ctlgrs6574988
GMAF0.06382
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21254220OA-icon.png]
Trait
Title Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Risk Allele
P-val 0.000004
Odds Ratio None None