rs74315496

Orientation

plus

Stabilized

plus

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

Make rs74315496(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

29661313

Gene

NF2

is a	snp
is	mentioned by
dbSNP	rs74315496
dbSNP (classic)	rs74315496
ClinGen	rs74315496
ebi	rs74315496
HLI	rs74315496
Exac	rs74315496
Gnomad	rs74315496
Varsome	rs74315496
LitVar	rs74315496
Map	rs74315496
PheGenI	rs74315496
Biobank	rs74315496
1000 genomes	rs74315496
hgdp	rs74315496
ensembl	rs74315496
geneview	rs74315496
scholar	rs74315496
google	rs74315496
pharmgkb	rs74315496
gwascentral	rs74315496
openSNP	rs74315496
23andMe	rs74315496
SNPshot	rs74315496
SNPdbe	rs74315496
MSV3d	rs74315496
GWAS Ctlg	rs74315496

Max Magnitude

7.5

OMIM	607379
Desc
Variant	0009
Related	also

ClinVar
Risk	rs74315496(T;T)
Alt	rs74315496(T;T)
Reference	Rs74315496(C;C)
Significance	Pathogenic
Disease	Neurofibromatosis
Variation	info
Gene	NF2
CLNDBN	Neurofibromatosis, type 2
Reversed	0
HGVS	NC_000022.10:g.30057302C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003451.2,