rs13397985

Orientation

plus

Stabilized

plus

Make rs13397985(G;G)

Make rs13397985(G;T)

Make rs13397985(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

230226508

Gene	SP110, SP140

is a	snp
is	mentioned by
dbSNP	rs13397985
dbSNP (classic)	rs13397985
ClinGen	rs13397985
ebi	rs13397985
HLI	rs13397985
Exac	rs13397985
Gnomad	rs13397985
Varsome	rs13397985
LitVar	rs13397985
Map	rs13397985
PheGenI	rs13397985
Biobank	rs13397985
1000 genomes	rs13397985
hgdp	rs13397985
ensembl	rs13397985
geneview	rs13397985
scholar	rs13397985
google	rs13397985
pharmgkb	rs13397985
gwascentral	rs13397985
openSNP	rs13397985
23andMe	rs13397985
SNPshot	rs13397985
SNPdbe	rs13397985
MSV3d	rs13397985
GWAS Ctlg	rs13397985

GMAF

0.1139

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

23andMe blog chronic lymphocytic leukemia

• rs13397985 G 1.41

GWAS
SNP	rs13397985
PubMedID	[PMID 18758461]
Condition	Chronic lymphocytic leukemia
Gene	SP140, SP110
Risk Allele	G
pValue	6.00E-010
OR	1.41
95% CI	1.26-1.57

[PMID 20855867] Inherited genetic susceptibility to monoclonal B-cell lymphocytosis

[PMID 19620980] Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.

[PMID 20731705] Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong.

GWAS snp
PMID	[PMID 22700719]
Trait
Title	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
Risk Allele
P-val	2E-7
Odds Ratio	1.3900 None

GWAS snp
PMID	[PMID 23770605]
Trait	Chronic lymphocytic leukemia
Title	Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Risk Allele	G
P-val	1E-22
Odds Ratio	1.45 [NR]

[PMID 23455380] Risk of genome-wide association study-identified genetic variants for non-Hodgkin lymphoma in a Chinese population.

GWAS snp
PMID	[PMID 24292274]
Trait	Chronic lymphocytic leukemia
Title	A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
Risk Allele	G
P-val	5E-13
Odds Ratio	1.43 [NR]