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rs121434259

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121434259(C;T)
Make rs121434259(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position29636805
GeneNF2
is asnp
is mentioned by
dbSNPrs121434259
ebirs121434259
HLIrs121434259
Exacrs121434259
Varsomers121434259
Maprs121434259
PheGenIrs121434259
hapmaprs121434259
1000 genomesrs121434259
hgdprs121434259
ensemblrs121434259
gopubmedrs121434259
geneviewrs121434259
scholarrs121434259
googlers121434259
pharmgkbrs121434259
gwascentralrs121434259
openSNPrs121434259
23andMers121434259
23andMe allrs121434259
SNP Nexus

SNPshotrs121434259
SNPdbers121434259
MSV3drs121434259
GWAS Ctlgrs121434259
Max Magnitude0
OMIM607379
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121434259(T;T)
Alt rs121434259(T;T)
Reference rs121434259(C;C)
Significance Pathogenic
Disease Meningioma
Variation info
Gene NF2
CLNDBN Meningioma
Reversed 0
HGVS NC_000022.10:g.30032794C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003446.4,