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rs26868

From SNPedia

Orientationminus
Stabilizedminus
Make rs26868(A;A)
Make rs26868(A;T)
Make rs26868(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position2199375
is asnp
is mentioned by
dbSNPrs26868
dbSNP (classic)rs26868
ClinGenrs26868
ebirs26868
HLIrs26868
Exacrs26868
Gnomadrs26868
Varsomers26868
LitVarrs26868
Maprs26868
PheGenIrs26868
Biobankrs26868
1000 genomesrs26868
hgdprs26868
ensemblrs26868
geneviewrs26868
scholarrs26868
googlers26868
pharmgkbrs26868
gwascentralrs26868
openSNPrs26868
23andMers26868
SNPshotrs26868
SNPdbers26868
MSV3drs26868
GWAS Ctlgrs26868
GMAF0.3664
Max Magnitude0
? (A;A) (A;T) (T;T) 28


GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height
Risk Allele A
P-val 9E-17
Odds Ratio 0.03 [NR] unit increase