rs16962638

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs16962638(A;G)

Make rs16962638(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

103534569

is a	snp
is	mentioned by
dbSNP	rs16962638
dbSNP (classic)	rs16962638
ClinGen	rs16962638
ebi	rs16962638
HLI	rs16962638
Exac	rs16962638
Gnomad	rs16962638
Varsome	rs16962638
LitVar	rs16962638
Map	rs16962638
PheGenI	rs16962638
Biobank	rs16962638
1000 genomes	rs16962638
hgdp	rs16962638
ensembl	rs16962638
geneview	rs16962638
scholar	rs16962638
google	rs16962638
pharmgkb	rs16962638
gwascentral	rs16962638
openSNP	rs16962638
23andMe	rs16962638
SNPshot	rs16962638
SNPdbe	rs16962638
MSV3d	rs16962638
GWAS Ctlg	rs16962638

GMAF

0.02755

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21901158]
Trait
Title	Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
Risk Allele	C
P-val	0.000006
Odds Ratio	15.0000 [8.00 - 22.00] % increase