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rs587776562

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776562(G;T)
Make rs587776562(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position29636877
GeneNF2
is asnp
is mentioned by
dbSNPrs587776562
ebirs587776562
HLIrs587776562
Exacrs587776562
Varsomers587776562
Maprs587776562
PheGenIrs587776562
hapmaprs587776562
1000 genomesrs587776562
hgdprs587776562
ensemblrs587776562
gopubmedrs587776562
geneviewrs587776562
scholarrs587776562
googlers587776562
pharmgkbrs587776562
gwascentralrs587776562
openSNPrs587776562
23andMers587776562
23andMe allrs587776562
SNP Nexus

SNPshotrs587776562
SNPdbers587776562
MSV3drs587776562
GWAS Ctlgrs587776562
Max Magnitude0
ClinVar
Risk rs587776562(T;T)
Alt rs587776562(T;T)
Reference rs587776562(G;G)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF2
CLNDBN Neurofibromatosis, type 2
Reversed 0
HGVS NC_000022.10:g.30032866G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003444.2,