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rs1427407

From SNPedia

Orientationplus
Stabilizedplus
Make rs1427407(G;G)
Make rs1427407(G;T)
Make rs1427407(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position60490908
GeneBCL11A
is asnp
is mentioned by
dbSNPrs1427407
ebirs1427407
HLIrs1427407
Exacrs1427407
Varsomers1427407
Maprs1427407
PheGenIrs1427407
hapmaprs1427407
1000 genomesrs1427407
hgdprs1427407
ensemblrs1427407
gopubmedrs1427407
geneviewrs1427407
scholarrs1427407
googlers1427407
pharmgkbrs1427407
gwascentralrs1427407
openSNPrs1427407
23andMers1427407
23andMe allrs1427407
SNP Nexus

SNPshotrs1427407
SNPdbers1427407
MSV3drs1427407
GWAS Ctlgrs1427407
GMAF0.2011
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS
SNP rs1427407
PubMedID [PMID 17767159]
Condition F-cell distribution
Gene BCL11A
Risk Allele
pValue 6.00E-031
OR 13.1
95% CI NR) % of variance explaine



[PMID 19474294OA-icon.png] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.


GET Evidence
rs1427407
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.78125
summary