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rs7846385

From SNPedia

Orientationplus
Stabilizedplus
Make rs7846385(C;C)
Make rs7846385(C;T)
Make rs7846385(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position77247943
is asnp
is mentioned by
dbSNPrs7846385
ebirs7846385
HLIrs7846385
Exacrs7846385
Varsomers7846385
Maprs7846385
PheGenIrs7846385
hapmaprs7846385
1000 genomesrs7846385
hgdprs7846385
ensemblrs7846385
gopubmedrs7846385
geneviewrs7846385
scholarrs7846385
googlers7846385
pharmgkbrs7846385
gwascentralrs7846385
openSNPrs7846385
23andMers7846385
23andMe allrs7846385
SNP Nexus

SNPshotrs7846385
SNPdbers7846385
MSV3drs7846385
GWAS Ctlgrs7846385
GMAF0.2199
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 4.9999999999999998E-8
Odds Ratio 5.00 [3.24-6.76] % SD 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.


[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
rs7846385
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.25
summary