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

rs1071583

From SNPedia

Orientationplus
Stabilizedplus
Make rs1071583(C;C)
Make rs1071583(C;T)
Make rs1071583(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position134909954
GeneFCN1
is asnp
is mentioned by
dbSNPrs1071583
ebirs1071583
HLIrs1071583
Exacrs1071583
Varsomers1071583
Maprs1071583
PheGenIrs1071583
hapmaprs1071583
1000 genomesrs1071583
hgdprs1071583
ensemblrs1071583
gopubmedrs1071583
geneviewrs1071583
scholarrs1071583
googlers1071583
pharmgkbrs1071583
gwascentralrs1071583
openSNPrs1071583
23andMers1071583
23andMe allrs1071583
SNP Nexus

SNPshotrs1071583
SNPdbers1071583
MSV3drs1071583
GWAS Ctlgrs1071583
GMAF0.3627
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.