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rs36098294

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs36098294(C;T)
Make rs36098294(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position87227421
GeneCHMP2B, MIR4795
is asnp
is mentioned by
dbSNPrs36098294
ebirs36098294
HLIrs36098294
Exacrs36098294
Varsomers36098294
Maprs36098294
PheGenIrs36098294
hapmaprs36098294
1000 genomesrs36098294
hgdprs36098294
ensemblrs36098294
gopubmedrs36098294
geneviewrs36098294
scholarrs36098294
googlers36098294
pharmgkbrs36098294
gwascentralrs36098294
openSNPrs36098294
23andMers36098294
23andMe allrs36098294
SNP Nexus

SNPshotrs36098294
SNPdbers36098294
MSV3drs36098294
GWAS Ctlgrs36098294
GMAF0.004591
Max Magnitude0

[PMID 20412296] Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients