rs10738445

Orientation

plus

Stabilized

plus

Make rs10738445(A;A)

Make rs10738445(A;C)

Make rs10738445(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

16680140

Gene

BNC2

is a	snp
is	mentioned by
dbSNP	rs10738445
dbSNP (classic)	rs10738445
ClinGen	rs10738445
ebi	rs10738445
HLI	rs10738445
Exac	rs10738445
Gnomad	rs10738445
Varsome	rs10738445
LitVar	rs10738445
Map	rs10738445
PheGenI	rs10738445
Biobank	rs10738445
1000 genomes	rs10738445
hgdp	rs10738445
ensembl	rs10738445
geneview	rs10738445
scholar	rs10738445
google	rs10738445
pharmgkb	rs10738445
gwascentral	rs10738445
openSNP	rs10738445
23andMe	rs10738445
SNPshot	rs10738445
SNPdbe	rs10738445
MSV3d	rs10738445
GWAS Ctlg	rs10738445

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

rs10738445 is a SNP in an intron of the BNC2 gene on chromosome 9.

A GWAS study in Japanese and Han Chinese scoliosis patients found a significant (though small; odds ratio 1.21, p = 2.46 × 10e−13) association between rs10738445(A) and the disorder, and several lines of experiment evidence supported the hypothesis that increased BNC2 expression predisposes individuals to adolescent scoliosis (AIS).10.1016/j.ajhg.2015.06.012

[PMID 26211971] A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis

[PMID 28342042] Genetic variant of BNC2 gene is functionally associated with adolescent idiopathic scoliosis in Chinese population.