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rs1474563

From SNPedia

Orientationplus
Stabilizedplus
Make rs1474563(C;C)
Make rs1474563(C;T)
Make rs1474563(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position79393696
is asnp
is mentioned by
dbSNPrs1474563
ebirs1474563
HLIrs1474563
Exacrs1474563
Varsomers1474563
Maprs1474563
PheGenIrs1474563
hapmaprs1474563
1000 genomesrs1474563
hgdprs1474563
ensemblrs1474563
gopubmedrs1474563
geneviewrs1474563
scholarrs1474563
googlers1474563
pharmgkbrs1474563
gwascentralrs1474563
openSNPrs1474563
23andMers1474563
23andMe allrs1474563
SNP Nexus

SNPshotrs1474563
SNPdbers1474563
MSV3drs1474563
GWAS Ctlgrs1474563
GMAF0.3579
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele T
P-val 0.0000030000000000000001
Odds Ratio 3.50 [1.93-5.07] % SD taller


[PMID 21253569OA-icon.png] Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?


GET Evidence
rs1474563
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.366667
summary