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rs1549519

From SNPedia

Orientationminus
Stabilizedminus
Make rs1549519(A;A)
Make rs1549519(A;G)
Make rs1549519(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position55680426
is asnp
is mentioned by
dbSNPrs1549519
dbSNP (classic)rs1549519
ClinGenrs1549519
ebirs1549519
HLIrs1549519
Exacrs1549519
Gnomadrs1549519
Varsomers1549519
LitVarrs1549519
Maprs1549519
PheGenIrs1549519
Biobankrs1549519
1000 genomesrs1549519
hgdprs1549519
ensemblrs1549519
geneviewrs1549519
scholarrs1549519
googlers1549519
pharmgkbrs1549519
gwascentralrs1549519
openSNPrs1549519
23andMers1549519
SNPshotrs1549519
SNPdbers1549519
MSV3drs1549519
GWAS Ctlgrs1549519
GMAF0.4628
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22021425OA-icon.png]
Trait
Title Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe).
Risk Allele T
P-val 6E-9
Odds Ratio 0.0480 None