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rs4932178

From SNPedia

Orientationplus
Stabilizedplus
Make rs4932178(C;C)
Make rs4932178(C;T)
Make rs4932178(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position90868426
GeneFURIN
is asnp
is mentioned by
dbSNPrs4932178
dbSNP (old)rs4932178
ClinGenrs4932178
ebirs4932178
HLIrs4932178
Exacrs4932178
Gnomadrs4932178
Varsomers4932178
Maprs4932178
PheGenIrs4932178
Biobankrs4932178
1000 genomesrs4932178
hgdprs4932178
ensemblrs4932178
gopubmedrs4932178
geneviewrs4932178
scholarrs4932178
googlers4932178
pharmgkbrs4932178
gwascentralrs4932178
openSNPrs4932178
23andMers4932178
23andMe allrs4932178
SNP Nexus

SNPshotrs4932178
SNPdbers4932178
MSV3drs4932178
GWAS Ctlgrs4932178
GMAF0.2686
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21889147] Proprotein convertases in human atherosclerotic plaques: the overexpression of FURIN and its substrate cytokines BAFF and APRIL


[PMID 23568742] [Association between sequence variation of Furin gene and obesity in ethnic Kazakh from Xinjiang]


[PMID 26137475OA-icon.png] Single Nucleotide Polymorphism (rs4932178) in the P1 Promoter of FURIN Is Not Prognostic to Colon Cancer