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rs12073837

From SNPedia

Orientationplus
Stabilizedplus
Make rs12073837(C;C)
Make rs12073837(C;T)
Make rs12073837(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position220836863
GeneHLX-AS1
is asnp
is mentioned by
dbSNPrs12073837
ebirs12073837
HLIrs12073837
Exacrs12073837
Varsomers12073837
Maprs12073837
PheGenIrs12073837
hapmaprs12073837
1000 genomesrs12073837
hgdprs12073837
ensemblrs12073837
gopubmedrs12073837
geneviewrs12073837
scholarrs12073837
googlers12073837
pharmgkbrs12073837
gwascentralrs12073837
openSNPrs12073837
23andMers12073837
23andMe allrs12073837
SNP Nexus

SNPshotrs12073837
SNPdbers12073837
MSV3drs12073837
GWAS Ctlgrs12073837
GMAF0.258
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21326311]
Trait
Title Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
Risk Allele T
P-val 0.000002
Odds Ratio 1.3900 [0.82-1.96] unit increase