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rs967591

From SNPedia

Orientationplus
Stabilizedplus
Make rs967591(A;A)
Make rs967591(A;G)
Make rs967591(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position45406676
GeneCD3EAP, PPP1R13L
is asnp
is mentioned by
dbSNPrs967591
ebirs967591
HLIrs967591
Exacrs967591
Varsomers967591
Maprs967591
PheGenIrs967591
hapmaprs967591
1000 genomesrs967591
hgdprs967591
ensemblrs967591
gopubmedrs967591
geneviewrs967591
scholarrs967591
googlers967591
pharmgkbrs967591
gwascentralrs967591
openSNPrs967591
23andMers967591
23andMe allrs967591
SNP Nexus

SNPshotrs967591
SNPdbers967591
MSV3drs967591
GWAS Ctlgrs967591
GMAF0.2466
Max Magnitude

[PMID 20061190] ERCC1 haplotypes modify bladder cancer risk: A case-control study


[PMID 19734419OA-icon.png] A polymorphism in NFKB1 is associated with improved effect of interferon-{alpha} maintenance treatment of patients with multiple myeloma after high-dose treatment with stem cell support.


[PMID 21046104] The importance of a sub-region on chromosome 19q13.3 for prognosis of multiple myeloma patients after high-dose treatment and stem cell support: a linkage disequilibrium mapping in RAI and CD3EAP.


[PMID 22335888] A specific diplotype defined by PPP1R13L rs1970764, CD3EAP rs967591 and ERCC1 rs11615 and lung cancer risk in a Chinese population.


[PMID 23180017] PPP1R13L variant associated with prognosis for patients with rectal cancer.


[PMID 23775331] A functional variant at 19q13.3, rs967591G>A, is associated with shorter survival of early-stage lung cancer.


[PMID 26563375] Association and interaction of NFKB1 rs28362491 insertion/deletion ATTG polymorphism and PPP1R13L and CD3EAP related to lung cancer risk in a Chinese population