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rs41264871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs41264871(A;G)
Make rs41264871(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position205066599
GeneCNTN2
is asnp
is mentioned by
dbSNPrs41264871
ebirs41264871
HLIrs41264871
Exacrs41264871
Varsomers41264871
Maprs41264871
PheGenIrs41264871
hapmaprs41264871
1000 genomesrs41264871
hgdprs41264871
ensemblrs41264871
gopubmedrs41264871
geneviewrs41264871
scholarrs41264871
googlers41264871
pharmgkbrs41264871
gwascentralrs41264871
openSNPrs41264871
23andMers41264871
23andMe allrs41264871
SNP Nexus

SNPshotrs41264871
SNPdbers41264871
MSV3drs41264871
GWAS Ctlgrs41264871
GMAF0.006887
Max Magnitude0

[PMID 22462668] Single-nucleotide polymorphism of transient axonal glycoprotein-1 and its correlation with clinical features and prognosis in chronic inflammatory demyelinating polyneuropathy