rs587776563

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs587776563(-;-)

Make rs587776563(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

29668442

Gene

NF2

is a	snp
is	mentioned by
dbSNP	rs587776563
dbSNP (classic)	rs587776563
ClinGen	rs587776563
ebi	rs587776563
HLI	rs587776563
Exac	rs587776563
Gnomad	rs587776563
Varsome	rs587776563
LitVar	rs587776563
Map	rs587776563
PheGenI	rs587776563
Biobank	rs587776563
1000 genomes	rs587776563
hgdp	rs587776563
ensembl	rs587776563
geneview	rs587776563
scholar	rs587776563
google	rs587776563
pharmgkb	rs587776563
gwascentral	rs587776563
openSNP	rs587776563
23andMe	rs587776563
SNPshot	rs587776563
SNPdbe	rs587776563
MSV3d	rs587776563
GWAS Ctlg	rs587776563

Max Magnitude

0

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,