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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
dbSNP (classic)rs967417
ClinGenrs967417
ebirs967417
HLIrs967417
Exacrs967417
Gnomadrs967417
Varsomers967417
LitVarrs967417
Maprs967417
PheGenIrs967417
Biobankrs967417
1000 genomesrs967417
hgdprs967417
ensemblrs967417
geneviewrs967417
scholarrs967417
googlers967417
pharmgkbrs967417
gwascentralrs967417
openSNPrs967417
23andMers967417
SNPshotrs967417
SNPdbers967417
MSV3drs967417
GWAS Ctlgrs967417
GMAF0.4949
Max Magnitude0
? (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.