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rs757978

From SNPedia

Orientationminus
Stabilizedminus
Make rs757978(A;A)
Make rs757978(A;G)
Make rs757978(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position241431686
GeneFARP2
is asnp
is mentioned by
dbSNPrs757978
dbSNP (classic)rs757978
ClinGenrs757978
ebirs757978
HLIrs757978
Exacrs757978
Gnomadrs757978
Varsomers757978
LitVarrs757978
Maprs757978
PheGenIrs757978
Biobankrs757978
1000 genomesrs757978
hgdprs757978
ensemblrs757978
geneviewrs757978
scholarrs757978
googlers757978
pharmgkbrs757978
gwascentralrs757978
openSNPrs757978
23andMers757978
SNPshotrs757978
SNPdbers757978
MSV3drs757978
GWAS Ctlgrs757978
GMAF0.07851
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20062064OA-icon.png]
Trait Chronic lymphocytic leukemia
Title Common variants at 2q37.3, 8q24.21, 15q21.3 abd 16q24.1 influence chronic lymphocytic leukemia risk
Risk Allele A
P-val 2E-9
Odds Ratio 1.38 [1.25-1.56]


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


[PMID 18773191OA-icon.png] Genetic association analyses of non-synonymous single nucleotide polymorphisms in diabetic nephropathy.


[PMID 20667095OA-icon.png] Effects of MCF2L2, ADIPOQ and SOX2 genetic polymorphisms on the development of nephropathy in type 1 Diabetes Mellitus.

GWAS snp
PMID [PMID 22700719OA-icon.png]
Trait
Title Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
Risk Allele T
P-val 0.000003
Odds Ratio 1.4600 None


GWAS snp
PMID [PMID 23770605OA-icon.png]
Trait Chronic lymphocytic leukemia
Title Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Risk Allele A
P-val 1E-7
Odds Ratio 1.29 [NR]