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rs185819

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs185819(C;C)
Make rs185819(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32082290
GeneTNXB
is asnp
is mentioned by
dbSNPrs185819
dbSNP (classic)rs185819
ClinGenrs185819
ebirs185819
HLIrs185819
Exacrs185819
Gnomadrs185819
Varsomers185819
LitVarrs185819
Maprs185819
PheGenIrs185819
Biobankrs185819
1000 genomesrs185819
hgdprs185819
ensemblrs185819
geneviewrs185819
scholarrs185819
googlers185819
pharmgkbrs185819
gwascentralrs185819
openSNPrs185819
23andMers185819
SNPshotrs185819
SNPdbers185819
MSV3drs185819
GWAS Ctlgrs185819
GMAF0.4307
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 T
P-val 2.9999999999999997E-8
Odds Ratio 5.20 [3.44-6.96] % SD taller


[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


[PMID 20010834OA-icon.png] Genome-wide association study identifies five loci associated with lung function.


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



[PMID 23053960] Genome-wide pathway analysis of genome-wide association studies on systemic lupus erythematosus and rheumatoid arthritis.


ClinVar
Risk rs185819(A;A) rs185819(C;C)
Alt rs185819(A;A) rs185819(C;C)
Reference Rs185819(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene TNXB
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.32050067T>C
CLNSRC
CLNACC RCV000246888.1,