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rs2145998

From SNPedia

Orientationminus
Stabilizedminus
Make rs2145998(A;A)
Make rs2145998(A;T)
Make rs2145998(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position79361940
is asnp
is mentioned by
dbSNPrs2145998
ebirs2145998
HLIrs2145998
Exacrs2145998
Varsomers2145998
Maprs2145998
PheGenIrs2145998
hapmaprs2145998
1000 genomesrs2145998
hgdprs2145998
ensemblrs2145998
gopubmedrs2145998
geneviewrs2145998
scholarrs2145998
googlers2145998
pharmgkbrs2145998
gwascentralrs2145998
openSNPrs2145998
23andMers2145998
23andMe allrs2145998
SNP Nexus

SNPshotrs2145998
SNPdbers2145998
MSV3drs2145998
GWAS Ctlgrs2145998
GMAF0.4578
Max Magnitude
? (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 4E-13
Odds Ratio 0.03 [NR] unit decrease