rs6735786

Orientation

plus

Stabilized

plus

Make rs6735786(C;C)

Make rs6735786(C;T)

Make rs6735786(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

103153780

is a	snp
is	mentioned by
dbSNP	rs6735786
dbSNP (classic)	rs6735786
ClinGen	rs6735786
ebi	rs6735786
HLI	rs6735786
Exac	rs6735786
Gnomad	rs6735786
Varsome	rs6735786
LitVar	rs6735786
Map	rs6735786
PheGenI	rs6735786
Biobank	rs6735786
1000 genomes	rs6735786
hgdp	rs6735786
ensembl	rs6735786
geneview	rs6735786
scholar	rs6735786
google	rs6735786
pharmgkb	rs6735786
gwascentral	rs6735786
openSNP	rs6735786
23andMe	rs6735786
SNPshot	rs6735786
SNPdbe	rs6735786
MSV3d	rs6735786
GWAS Ctlg	rs6735786

GMAF

0.4036

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 19079262]
Trait	Bone mineral density (hip)
Title	New sequence variants associated with bone mineral density
Risk Allele	C
P-val	0.000002
Odds Ratio	0.07 [0.04-0.09] SD decrease