rs185819

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs185819(C;C)

Make rs185819(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

32082290

Gene

TNXB

is a	snp
is	mentioned by
dbSNP	rs185819
dbSNP (classic)	rs185819
ClinGen	rs185819
ebi	rs185819
HLI	rs185819
Exac	rs185819
Gnomad	rs185819
Varsome	rs185819
LitVar	rs185819
Map	rs185819
PheGenI	rs185819
Biobank	rs185819
1000 genomes	rs185819
hgdp	rs185819
ensembl	rs185819
geneview	rs185819
scholar	rs185819
google	rs185819
pharmgkb	rs185819
gwascentral	rs185819
openSNP	rs185819
23andMe	rs185819
SNPshot	rs185819
SNPdbe	rs185819
MSV3d	rs185819
GWAS Ctlg	rs185819

GMAF

0.4307

Max Magnitude

0

?	(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 19030899] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.

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

[PMID 20546612] 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,