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rs10491121

From SNPedia

Orientationplus
Stabilizedplus
Make rs10491121(A;A)
Make rs10491121(A;G)
Make rs10491121(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position36102943
GeneCCL4, LOC101927369
is asnp
is mentioned by
dbSNPrs10491121
dbSNP (classic)rs10491121
ClinGenrs10491121
ebirs10491121
HLIrs10491121
Exacrs10491121
Gnomadrs10491121
Varsomers10491121
LitVarrs10491121
Maprs10491121
PheGenIrs10491121
Biobankrs10491121
1000 genomesrs10491121
hgdprs10491121
ensemblrs10491121
geneviewrs10491121
scholarrs10491121
googlers10491121
pharmgkbrs10491121
gwascentralrs10491121
openSNPrs10491121
23andMers10491121
SNPshotrs10491121
SNPdbers10491121
MSV3drs10491121
GWAS Ctlgrs10491121
Max Magnitude0
? (A;A) (A;G) (G;G) 28


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[PMID 28824325OA-icon.png] Impacts of CCL4 gene polymorphisms on hepatocellular carcinoma susceptibility and development.


[PMID 30123055OA-icon.png] Correlation between CCL4 gene polymorphisms and clinical aspects of breast cancer.