rs587776564

Orientation

plus

Stabilized

plus

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

Make rs587776564(-;G)

Make rs587776564(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

29636761

Gene

NF2

is a	snp
is	mentioned by
dbSNP	rs587776564
dbSNP (classic)	rs587776564
ClinGen	rs587776564
ebi	rs587776564
HLI	rs587776564
Exac	rs587776564
Gnomad	rs587776564
Varsome	rs587776564
LitVar	rs587776564
Map	rs587776564
PheGenI	rs587776564
Biobank	rs587776564
1000 genomes	rs587776564
hgdp	rs587776564
ensembl	rs587776564
geneview	rs587776564
scholar	rs587776564
google	rs587776564
pharmgkb	rs587776564
gwascentral	rs587776564
openSNP	rs587776564
23andMe	rs587776564
SNPshot	rs587776564
SNPdbe	rs587776564
MSV3d	rs587776564
GWAS Ctlg	rs587776564

Max Magnitude

0

ClinVar
Risk	rs587776564(G;G)
Alt	rs587776564(G;G)
Reference	Rs587776564(-;-)
Significance	Pathogenic
Disease	Schwannomatosis 1
Variation	info
Gene	NF2
CLNDBN	Schwannomatosis 1
Reversed	0
HGVS	NC_000022.10:g.30032750_30032751insG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003460.5,