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rs5751614

From SNPedia

Orientationplus
Stabilizedplus
Make rs5751614(A;A)
Make rs5751614(A;G)
Make rs5751614(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position23250864
GeneBCR
is asnp
is mentioned by
dbSNPrs5751614
ebirs5751614
HLIrs5751614
Exacrs5751614
Varsomers5751614
Maprs5751614
PheGenIrs5751614
hapmaprs5751614
1000 genomesrs5751614
hgdprs5751614
ensemblrs5751614
gopubmedrs5751614
geneviewrs5751614
scholarrs5751614
googlers5751614
pharmgkbrs5751614
gwascentralrs5751614
openSNPrs5751614
23andMers5751614
23andMe allrs5751614
SNP Nexus

SNPshotrs5751614
SNPdbers5751614
MSV3drs5751614
GWAS Ctlgrs5751614
GMAF0.4559
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele A
P-val 0.0000060000000000000002
Odds Ratio 4.30 [2.34-6.26] % SD taller


GET Evidence
rs5751614
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.640625
summary