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rs9909416

From SNPedia

Orientationplus
Stabilizedplus
Make rs9909416(C;C)
Make rs9909416(C;T)
Make rs9909416(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position35870979
GeneLOC105371744
is asnp
is mentioned by
dbSNPrs9909416
dbSNP (classic)rs9909416
ClinGenrs9909416
ebirs9909416
HLIrs9909416
Exacrs9909416
Gnomadrs9909416
Varsomers9909416
LitVarrs9909416
Maprs9909416
PheGenIrs9909416
Biobankrs9909416
1000 genomesrs9909416
hgdprs9909416
ensemblrs9909416
geneviewrs9909416
scholarrs9909416
googlers9909416
pharmgkbrs9909416
gwascentralrs9909416
openSNPrs9909416
23andMers9909416
SNPshotrs9909416
SNPdbers9909416
MSV3drs9909416
GWAS Ctlgrs9909416
GMAF0.1997
Max Magnitude0
? (C;C) (C;T) (T;T) 28


OMIM187011
DescCHEMOKINE, CC MOTIF, LIGAND 5; CCL5
Variant
Relatedalso


[PMID 18217191] Association of CC chemokine ligand 5 genotype with urinary albumin excretion in the non-diabetic Japanese general population: the Takahata study.