rs6601327

Orientation

plus

Stabilized

plus

Make rs6601327(A;A)

Make rs6601327(A;G)

Make rs6601327(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

9538022

is a	snp
is	mentioned by
dbSNP	rs6601327
dbSNP (classic)	rs6601327
ClinGen	rs6601327
ebi	rs6601327
HLI	rs6601327
Exac	rs6601327
Gnomad	rs6601327
Varsome	rs6601327
LitVar	rs6601327
Map	rs6601327
PheGenI	rs6601327
Biobank	rs6601327
1000 genomes	rs6601327
hgdp	rs6601327
ensembl	rs6601327
geneview	rs6601327
scholar	rs6601327
google	rs6601327
pharmgkb	rs6601327
gwascentral	rs6601327
openSNP	rs6601327
23andMe	rs6601327
SNPshot	rs6601327
SNPdbe	rs6601327
MSV3d	rs6601327
GWAS Ctlg	rs6601327

GMAF

0.4885

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23502783]
Trait	Multiple myeloma (hyperdiploidy)
Title	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Risk Allele	G
P-val	8E-6
Odds Ratio	1.27 [1.14-1.41]