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rs798544

From SNPedia

Orientationminus
Stabilizedminus
Make rs798544(A;A)
Make rs798544(A;G)
Make rs798544(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position2723468
GeneLOC100996298
is asnp
is mentioned by
dbSNPrs798544
ebirs798544
HLIrs798544
Exacrs798544
Varsomers798544
Maprs798544
PheGenIrs798544
hapmaprs798544
1000 genomesrs798544
hgdprs798544
ensemblrs798544
gopubmedrs798544
geneviewrs798544
scholarrs798544
googlers798544
pharmgkbrs798544
gwascentralrs798544
openSNPrs798544
23andMers798544
23andMe allrs798544
SNP Nexus

SNPshotrs798544
SNPdbers798544
MSV3drs798544
GWAS Ctlgrs798544
GMAF0.2415
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs798544
PubMedID [PMID 18391951]
Condition Height
Gene GNA12
Risk Allele G
pValue 7.00E-015
OR 5.9
95% CI 6.03-8.77) % SD talle



[PMID 17357082OA-icon.png] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

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

[PMID 19197348OA-icon.png] Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.

[PMID 20017971OA-icon.png] Assessing the impact of global versus local ancestry in association studies.

[PMID 20546612OA-icon.png] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.


GET Evidence
rs798544
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.230159
summary