rs121434259

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(C;T)	7.5	Neurofibromatosis, type 2

Make rs121434259(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

29636805

Gene

NF2

is a	snp
is	mentioned by
dbSNP	rs121434259
dbSNP (classic)	rs121434259
ClinGen	rs121434259
ebi	rs121434259
HLI	rs121434259
Exac	rs121434259
Gnomad	rs121434259
Varsome	rs121434259
LitVar	rs121434259
Map	rs121434259
PheGenI	rs121434259
Biobank	rs121434259
1000 genomes	rs121434259
hgdp	rs121434259
ensembl	rs121434259
geneview	rs121434259
scholar	rs121434259
google	rs121434259
pharmgkb	rs121434259
gwascentral	rs121434259
openSNP	rs121434259
23andMe	rs121434259
SNPshot	rs121434259
SNPdbe	rs121434259
MSV3d	rs121434259
GWAS Ctlg	rs121434259

Max Magnitude

7.5

OMIM	607379
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121434259(T;T)
Alt	rs121434259(T;T)
Reference	Rs121434259(C;C)
Significance	Pathogenic
Disease	Meningioma not provided
Variation	info
Gene	NF2
CLNDBN	Meningioma not provided
Reversed	0
HGVS	NC_000022.10:g.30032794C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003446.4, RCV000255708.1,