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rs587776565

From SNPedia

Orientationplus
Geno Mag Summary
(AAGGACA;AAGGACA) 0 common in clinvar
Make rs587776565(-;-)
Make rs587776565(-;AAGGACA)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position29636841
GeneNF2
is asnp
is mentioned by
dbSNPrs587776565
ebirs587776565
HLIrs587776565
Exacrs587776565
Varsomers587776565
Maprs587776565
PheGenIrs587776565
hapmaprs587776565
1000 genomesrs587776565
hgdprs587776565
ensemblrs587776565
gopubmedrs587776565
geneviewrs587776565
scholarrs587776565
googlers587776565
pharmgkbrs587776565
gwascentralrs587776565
openSNPrs587776565
23andMers587776565
23andMe allrs587776565
SNP Nexus

SNPshotrs587776565
SNPdbers587776565
MSV3drs587776565
GWAS Ctlgrs587776565
Max Magnitude0
ClinVar
Risk rs587776565(;)
Alt rs587776565(;)
Reference rs587776565(AAGGACA;AAGGACA)
Significance Pathogenic
Disease Schwannomatosis
Variation info
Gene NF2
CLNDBN Schwannomatosis
Reversed 0
HGVS NC_000022.10:g.30032830_30032836delAAGGACA
CLNSRC OMIM Allelic Variant
CLNACC RCV000003461.4,