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rs17549193

From SNPedia

Orientationplus
Stabilizedplus
Make rs17549193(C;C)
Make rs17549193(C;T)
Make rs17549193(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position134887180
GeneFCN2
is asnp
is mentioned by
dbSNPrs17549193
ebirs17549193
HLIrs17549193
Exacrs17549193
Varsomers17549193
Maprs17549193
PheGenIrs17549193
hapmaprs17549193
1000 genomesrs17549193
hgdprs17549193
ensemblrs17549193
gopubmedrs17549193
geneviewrs17549193
scholarrs17549193
googlers17549193
pharmgkbrs17549193
gwascentralrs17549193
openSNPrs17549193
23andMers17549193
23andMe allrs17549193
SNP Nexus

SNPshotrs17549193
SNPdbers17549193
MSV3drs17549193
GWAS Ctlgrs17549193
GMAF0.241
Max Magnitude
OMIM601624
DescFICOLIN 2; FCN2
Variant
Relatedalso
[PMID 17680820OA-icon.png] Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 gene.

[PMID 19220833OA-icon.png] Exploring the role of polymorphisms in ficolin genes in respiratory tract infections in children.


GET Evidence
FCN2-T236M
aa_change Thr236Met
aa_change_short T236M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.308143
summary



[PMID 22848725OA-icon.png] Mannose-binding lectin deficiency is associated with myocardial infarction: the HUNT2 study in Norway.


[PMID 23525825OA-icon.png] Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.