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rs2989727

From SNPedia

Orientationplus
Stabilizedplus
Make rs2989727(C;C)
Make rs2989727(C;T)
Make rs2989727(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position134919852
GeneFCN1
is asnp
is mentioned by
dbSNPrs2989727
dbSNP (old)rs2989727
ClinGenrs2989727
ebirs2989727
HLIrs2989727
Exacrs2989727
Varsomers2989727
Maprs2989727
PheGenIrs2989727
Biobankrs2989727
1000 genomesrs2989727
hgdprs2989727
ensemblrs2989727
gopubmedrs2989727
geneviewrs2989727
scholarrs2989727
googlers2989727
pharmgkbrs2989727
gwascentralrs2989727
openSNPrs2989727
23andMers2989727
23andMe allrs2989727
SNP Nexus

SNPshotrs2989727
SNPdbers2989727
MSV3drs2989727
GWAS Ctlgrs2989727
GMAF0.478
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 18032536] the A allele rs2989727 was significantly increased in RA patients (67%) compared with controls (60%) (P = 0.002). Also, the frequency of the G allele of rs1071583 was increased in RA patients (68%) compared with controls (61%) (P = 0.003).


[PMID 22940091] Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients.


[PMID 22941510] Susceptibility to leprosy is associated with M-ficolin polymorphisms.