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rs2072446

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2072446(C;T)
Make rs2072446(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position49510457
GeneNGFR
is asnp
is mentioned by
dbSNPrs2072446
ebirs2072446
HLIrs2072446
Exacrs2072446
Varsomers2072446
Maprs2072446
PheGenIrs2072446
hapmaprs2072446
1000 genomesrs2072446
hgdprs2072446
ensemblrs2072446
gopubmedrs2072446
geneviewrs2072446
scholarrs2072446
googlers2072446
pharmgkbrs2072446
gwascentralrs2072446
openSNPrs2072446
23andMers2072446
23andMe allrs2072446
SNP Nexus

SNPshotrs2072446
SNPdbers2072446
MSV3drs2072446
GWAS Ctlgrs2072446
GMAF0.06152
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 22468730] Multilocus Analysis of Candidate Genes Involved in Neurogenic Inflammation in Pediatric Asthma and Related Phenotypes: A Case-Control Study


[PMID 17212826OA-icon.png] TAMGeS: a Three-array Method for Genotyping of SNPs by a dual-colour approach.


[PMID 18780967] SNPs in neurotrophin system genes and Alzheimer's disease in an Italian population.


GET Evidence
NGFR-S205L
aa_change Ser205Leu
aa_change_short S205L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0395055
summary



[PMID 25227100] Selection of human p75NTR tag SNPs and its biological significance for clinical association studies


[PMID 26254621] Association between genetic variants related to glutamatergic, dopaminergic and neurodevelopment pathways and white matter microstructure in child and adolescent patients with obsessive-compulsive disorder