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rs587776564

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776564(-;-)
Make rs587776564(-;G)
Make rs587776564(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position29636761
GeneNF2
is asnp
is mentioned by
dbSNPrs587776564
ebirs587776564
HLIrs587776564
Exacrs587776564
Varsomers587776564
Maprs587776564
PheGenIrs587776564
hapmaprs587776564
1000 genomesrs587776564
hgdprs587776564
ensemblrs587776564
gopubmedrs587776564
geneviewrs587776564
scholarrs587776564
googlers587776564
pharmgkbrs587776564
gwascentralrs587776564
openSNPrs587776564
23andMers587776564
23andMe allrs587776564
SNP Nexus

SNPshotrs587776564
SNPdbers587776564
MSV3drs587776564
GWAS Ctlgrs587776564
Max Magnitude0
ClinVar
Risk rs587776564(G;G)
Alt rs587776564(G;G)
Reference rs587776564(;)
Significance Pathogenic
Disease Schwannomatosis
Variation info
Gene NF2
CLNDBN Schwannomatosis
Reversed 0
HGVS NC_000022.10:g.30032750_30032751insG
CLNSRC OMIM Allelic Variant
CLNACC RCV000003460.5,