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rs757608

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Orientationminus
Stabilizedminus
Make rs757608(C;C)
Make rs757608(C;T)
Make rs757608(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position61419916
is asnp
is mentioned by
dbSNPrs757608
ebirs757608
HLIrs757608
Exacrs757608
Varsomers757608
Maprs757608
PheGenIrs757608
hapmaprs757608
1000 genomesrs757608
hgdprs757608
ensemblrs757608
gopubmedrs757608
geneviewrs757608
scholarrs757608
googlers757608
pharmgkbrs757608
gwascentralrs757608
openSNPrs757608
23andMers757608
23andMe allrs757608
SNP Nexus

SNPshotrs757608
SNPdbers757608
MSV3drs757608
GWAS Ctlgrs757608
GMAF0.2897
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 T
P-val 5.9999999999999995E-8
Odds Ratio 4.40 [2.83-5.97] % 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 20027299OA-icon.png] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.


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


GET Evidence
rs757608
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.734375
summary