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rs4796195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs4796195(A;G)
Make rs4796195(G;G)
ReferenceGRCh37 37.1/131
Chromosome17
Position34539882
GeneCCL4L1
is asnp
is mentioned by
dbSNPrs4796195
ebirs4796195
HLIrs4796195
Exacrs4796195
Varsomers4796195
Maprs4796195
PheGenIrs4796195
hapmaprs4796195
1000 genomesrs4796195
hgdprs4796195
ensemblrs4796195
gopubmedrs4796195
geneviewrs4796195
scholarrs4796195
googlers4796195
pharmgkbrs4796195
gwascentralrs4796195
openSNPrs4796195
23andMers4796195
23andMe allrs4796195
SNP Nexus

SNPshotrs4796195
SNPdbers4796195
MSV3drs4796195
GWAS Ctlgrs4796195
Max Magnitude0
[PMID 19148142] Copy number variation associated with susceptibility rejection in lung transplantation. The CNV and rs4796195 demonstrate the effect is mainly due to the cnv.


[PMID 17848170OA-icon.png] The chemokine network. II. On how polymorphisms and alternative splicing increase the number of molecular species and configure intricate patterns of disease susceptibility.


[PMID 18368065] Population structure in copy number variation and SNPs in the CCL4L chemokine gene.


[PMID 21614014] CCL4L polymorphisms and CCL4/CCL4L serum levels are associated with psoriasis severity.