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rs8007661

From SNPedia

Orientationplus
Stabilizedplus
Make rs8007661(C;C)
Make rs8007661(C;T)
Make rs8007661(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position91993614
GeneTRIP11
is asnp
is mentioned by
dbSNPrs8007661
ebirs8007661
HLIrs8007661
Exacrs8007661
Varsomers8007661
Maprs8007661
PheGenIrs8007661
hapmaprs8007661
1000 genomesrs8007661
hgdprs8007661
ensemblrs8007661
gopubmedrs8007661
geneviewrs8007661
scholarrs8007661
googlers8007661
pharmgkbrs8007661
gwascentralrs8007661
openSNPrs8007661
23andMers8007661
23andMe allrs8007661
SNP Nexus

SNPshotrs8007661
SNPdbers8007661
MSV3drs8007661
GWAS Ctlgrs8007661
GMAF0.4821
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs8007661
PubMedID [PMID 18391950OA-icon.png]
Condition Height
Gene TRIP11,ATXN3
Risk Allele T
pValue 6.00E-010
OR 0.42
95% CI 0.30-0.54) cm shorte



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


GET Evidence
rs8007661
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.595238
summary