Have questions? Visit https://www.reddit.com/r/SNPedia

rs12449568

From SNPedia

Orientationplus
Stabilizedplus
Make rs12449568(C;C)
Make rs12449568(C;T)
Make rs12449568(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position56352794
GeneANKFN1
is asnp
is mentioned by
dbSNPrs12449568
ebirs12449568
HLIrs12449568
Exacrs12449568
Varsomers12449568
Maprs12449568
PheGenIrs12449568
hapmaprs12449568
1000 genomesrs12449568
hgdprs12449568
ensemblrs12449568
gopubmedrs12449568
geneviewrs12449568
scholarrs12449568
googlers12449568
pharmgkbrs12449568
gwascentralrs12449568
openSNPrs12449568
23andMers12449568
23andMe allrs12449568
SNP Nexus

SNPshotrs12449568
SNPdbers12449568
MSV3drs12449568
GWAS Ctlgrs12449568
GMAF0.4669
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391950OA-icon.png]
Trait Height
Title Identification of ten loci associated with height highlights new biological pathways in human growth
Risk Allele C
P-val 0.0000019999999999999999
Odds Ratio 0.25 [0.15-0.35] cm taller


[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


[PMID 19039035OA-icon.png] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.


GET Evidence
rs12449568
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.4375
summary