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rs757978

From SNPedia

Orientationminus
Stabilizedplus
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
ebirs757978
HLIrs757978
Exacrs757978
Varsomers757978
Maprs757978
PheGenIrs757978
hapmaprs757978
1000 genomesrs757978
hgdprs757978
ensemblrs757978
gopubmedrs757978
geneviewrs757978
scholarrs757978
googlers757978
pharmgkbrs757978
gwascentralrs757978
openSNPrs757978
23andMers757978
23andMe allrs757978
SNP Nexus

SNPshotrs757978
SNPdbers757978
MSV3drs757978
GWAS Ctlgrs757978
GMAF0.07851
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20062064]
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


GET Evidence
FARP2-T260I
aa_change Thr260Ile
aa_change_short T260I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.107269
summary



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]