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rs10799445

From SNPedia

Orientationplus
Stabilizedplus
Make rs10799445(A;A)
Make rs10799445(A;C)
Make rs10799445(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position227724182
is asnp
is mentioned by
dbSNPrs10799445
ebirs10799445
HLIrs10799445
Exacrs10799445
Varsomers10799445
Maprs10799445
PheGenIrs10799445
hapmaprs10799445
1000 genomesrs10799445
hgdprs10799445
ensemblrs10799445
gopubmedrs10799445
geneviewrs10799445
scholarrs10799445
googlers10799445
pharmgkbrs10799445
gwascentralrs10799445
openSNPrs10799445
23andMers10799445
23andMe allrs10799445
SNP Nexus

SNPshotrs10799445
SNPdbers10799445
MSV3drs10799445
GWAS Ctlgrs10799445
GMAF0.2378
Max Magnitude
? (A;A) (A;C) (C;C) 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 2E-13
Odds Ratio .03 [NR] unit increase