rs74315495

Orientation

plus

Stabilized

plus

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

Make rs74315495(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

29655621

Gene

NF2

is a	snp
is	mentioned by
dbSNP	rs74315495
dbSNP (classic)	rs74315495
ClinGen	rs74315495
ebi	rs74315495
HLI	rs74315495
Exac	rs74315495
Gnomad	rs74315495
Varsome	rs74315495
LitVar	rs74315495
Map	rs74315495
PheGenI	rs74315495
Biobank	rs74315495
1000 genomes	rs74315495
hgdp	rs74315495
ensembl	rs74315495
geneview	rs74315495
scholar	rs74315495
google	rs74315495
pharmgkb	rs74315495
gwascentral	rs74315495
openSNP	rs74315495
23andMe	rs74315495
SNPshot	rs74315495
SNPdbe	rs74315495
MSV3d	rs74315495
GWAS Ctlg	rs74315495

Max Magnitude

7.5

OMIM	607379
Desc
Variant	0008
Related	also

ClinVar
Risk	rs74315495(T;T)
Alt	rs74315495(T;T)
Reference	Rs74315495(G;G)
Significance	Pathogenic
Disease	Neurofibromatosis
Variation	info
Gene	NF2
CLNDBN	Neurofibromatosis, type 2
Reversed	0
HGVS	NC_000022.10:g.30051610G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003450.2,