rs7144018

Orientation

plus

Stabilized

plus

Make rs7144018(C;C)

Make rs7144018(C;T)

Make rs7144018(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

57140349

is a	snp
is	mentioned by
dbSNP	rs7144018
dbSNP (classic)	rs7144018
ClinGen	rs7144018
ebi	rs7144018
HLI	rs7144018
Exac	rs7144018
Gnomad	rs7144018
Varsome	rs7144018
LitVar	rs7144018
Map	rs7144018
PheGenI	rs7144018
Biobank	rs7144018
1000 genomes	rs7144018
hgdp	rs7144018
ensembl	rs7144018
geneview	rs7144018
scholar	rs7144018
google	rs7144018
pharmgkb	rs7144018
gwascentral	rs7144018
openSNP	rs7144018
23andMe	rs7144018
SNPshot	rs7144018
SNPdbe	rs7144018
MSV3d	rs7144018
GWAS Ctlg	rs7144018

GMAF

0.258

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23502783]
Trait	Multiple myeloma (IgH translocation)
Title	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Risk Allele	G
P-val	9E-6
Odds Ratio	1.85 [1.41-2.44]