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rs878853925

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853925(A;T)
Make rs878853925(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position29681491
GeneNF2
is asnp
is mentioned by
dbSNPrs878853925
ebirs878853925
HLIrs878853925
Exacrs878853925
Varsomers878853925
Maprs878853925
PheGenIrs878853925
hapmaprs878853925
1000 genomesrs878853925
hgdprs878853925
ensemblrs878853925
gopubmedrs878853925
geneviewrs878853925
scholarrs878853925
googlers878853925
pharmgkbrs878853925
gwascentralrs878853925
openSNPrs878853925
23andMers878853925
23andMe allrs878853925
SNP Nexus

SNPshotrs878853925
SNPdbers878853925
MSV3drs878853925
GWAS Ctlgrs878853925
Max Magnitude0
ClinVar
Risk rs878853925(T;T)
Alt rs878853925(T;T)
Reference rs878853925(A;A)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF2
CLNDBN Neurofibromatosis, type 2
Reversed 0
HGVS NC_000022.10:g.30077480A>T
CLNSRC
CLNACC RCV000232701.1,