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

rs967417

From SNPedia

Orientationminus
Stabilizedminus
Make rs967417(C;C)
Make rs967417(C;T)
Make rs967417(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position6640246
is asnp
is mentioned by
dbSNPrs967417
ebirs967417
HLIrs967417
Exacrs967417
Varsomers967417
Maprs967417
PheGenIrs967417
hapmaprs967417
1000 genomesrs967417
hgdprs967417
ensemblrs967417
gopubmedrs967417
geneviewrs967417
scholarrs967417
googlers967417
pharmgkbrs967417
gwascentralrs967417
openSNPrs967417
23andMers967417
23andMe allrs967417
SNP Nexus

SNPshotrs967417
SNPdbers967417
MSV3drs967417
GWAS Ctlgrs967417
GMAF0.4949
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 C
P-val 2E-8
Odds Ratio 4.30 [2.73-5.87] % SD taller


[PMID 17186469OA-icon.png] Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.


[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
rs967417
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.40625
summary