rs587776565

Orientation

plus

Stabilized

plus

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

Make rs587776565(-;-)

Make rs587776565(-;AAGGACA)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

29636841

Gene

NF2

is a	snp
is	mentioned by
dbSNP	rs587776565
dbSNP (classic)	rs587776565
ClinGen	rs587776565
ebi	rs587776565
HLI	rs587776565
Exac	rs587776565
Gnomad	rs587776565
Varsome	rs587776565
LitVar	rs587776565
Map	rs587776565
PheGenI	rs587776565
Biobank	rs587776565
1000 genomes	rs587776565
hgdp	rs587776565
ensembl	rs587776565
geneview	rs587776565
scholar	rs587776565
google	rs587776565
pharmgkb	rs587776565
gwascentral	rs587776565
openSNP	rs587776565
23andMe	rs587776565
SNPshot	rs587776565
SNPdbe	rs587776565
MSV3d	rs587776565
GWAS Ctlg	rs587776565

Max Magnitude

0

ClinVar
Risk	rs587776565(-;-)
Alt	rs587776565(-;-)
Reference	Rs587776565(AAGGACA;AAGGACA)
Significance	Pathogenic
Disease	Schwannomatosis 1
Variation	info
Gene	NF2
CLNDBN	Schwannomatosis 1
Reversed	0
HGVS	NC_000022.10:g.30032830_30032836delAAGGACA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003461.4,