Have questions? Visit https://www.reddit.com/r/SNPedia

rs2994809

From SNPedia

Orientationplus
Stabilizedplus
Make rs2994809(C;C)
Make rs2994809(C;T)
Make rs2994809(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position119809354
GeneREG4
is asnp
is mentioned by
dbSNPrs2994809
dbSNP (old)rs2994809
ClinGenrs2994809
ebirs2994809
HLIrs2994809
Exacrs2994809
Gnomadrs2994809
Varsomers2994809
Maprs2994809
PheGenIrs2994809
Biobankrs2994809
1000 genomesrs2994809
hgdprs2994809
ensemblrs2994809
gopubmedrs2994809
geneviewrs2994809
scholarrs2994809
googlers2994809
pharmgkbrs2994809
gwascentralrs2994809
openSNPrs2994809
23andMers2994809
23andMe allrs2994809
SNP Nexus

SNPshotrs2994809
SNPdbers2994809
MSV3drs2994809
GWAS Ctlgrs2994809
GMAF0.1777
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23650115] Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility and clinical outcome