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

rs2274064

From SNPedia

Orientationplus
Stabilizedplus
Make rs2274064(C;C)
Make rs2274064(C;T)
Make rs2274064(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position183573252
GeneNCF2
is asnp
is mentioned by
dbSNPrs2274064
ebirs2274064
HLIrs2274064
Exacrs2274064
Varsomers2274064
Maprs2274064
PheGenIrs2274064
hapmaprs2274064
1000 genomesrs2274064
hgdprs2274064
ensemblrs2274064
gopubmedrs2274064
geneviewrs2274064
scholarrs2274064
googlers2274064
pharmgkbrs2274064
gwascentralrs2274064
openSNPrs2274064
23andMers2274064
23andMe allrs2274064
SNP Nexus

SNPshotrs2274064
SNPdbers2274064
MSV3drs2274064
GWAS Ctlgrs2274064
Merged fromRs34730753
GMAF0.4977
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 16608528OA-icon.png] Genetic polymorphisms and susceptibility to lung disease.


GET Evidence
NCF2-K136R
aa_change Lys136Arg
aa_change_short K136R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency
summary