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rs587776563

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776563(-;-)
Make rs587776563(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position29668442
GeneNF2
is asnp
is mentioned by
dbSNPrs587776563
ebirs587776563
HLIrs587776563
Exacrs587776563
Varsomers587776563
Maprs587776563
PheGenIrs587776563
hapmaprs587776563
1000 genomesrs587776563
hgdprs587776563
ensemblrs587776563
gopubmedrs587776563
geneviewrs587776563
scholarrs587776563
googlers587776563
pharmgkbrs587776563
gwascentralrs587776563
openSNPrs587776563
23andMers587776563
23andMe allrs587776563
SNP Nexus

SNPshotrs587776563
SNPdbers587776563
MSV3drs587776563
GWAS Ctlgrs587776563
Max Magnitude0
ClinVar
Risk rs587776563(;)
Alt rs587776563(;)
Reference rs587776563(A;A)
Significance Pathogenic
Disease Meningioma
Variation info
Gene NF2
CLNDBN Meningioma
Reversed 0
HGVS NC_000022.10:g.30064431delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000003445.4,