rs891088

Orientation

plus

Stabilized

plus

Make rs891088(A;A)

Make rs891088(A;G)

Make rs891088(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

7184751

Gene

INSR

is a	snp
is	mentioned by
dbSNP	rs891088
dbSNP (classic)	rs891088
ClinGen	rs891088
ebi	rs891088
HLI	rs891088
Exac	rs891088
Gnomad	rs891088
Varsome	rs891088
LitVar	rs891088
Map	rs891088
PheGenI	rs891088
Biobank	rs891088
1000 genomes	rs891088
hgdp	rs891088
ensembl	rs891088
geneview	rs891088
scholar	rs891088
google	rs891088
pharmgkb	rs891088
gwascentral	rs891088
openSNP	rs891088
23andMe	rs891088
SNPshot	rs891088
SNPdbe	rs891088
MSV3d	rs891088
GWAS Ctlg	rs891088

GMAF

0.3007

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 20881960]
Trait
Title	Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele	A
P-val	2E-12
Odds Ratio	0.0300 [NR] meters decrease