rs74315498

Orientation

plus

Stabilized

plus

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

Make rs74315498(C;T)

Make rs74315498(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

29671910

Gene

NF2

is a	snp
is	mentioned by
dbSNP	rs74315498
dbSNP (classic)	rs74315498
ClinGen	rs74315498
ebi	rs74315498
HLI	rs74315498
Exac	rs74315498
Gnomad	rs74315498
Varsome	rs74315498
LitVar	rs74315498
Map	rs74315498
PheGenI	rs74315498
Biobank	rs74315498
1000 genomes	rs74315498
hgdp	rs74315498
ensembl	rs74315498
geneview	rs74315498
scholar	rs74315498
google	rs74315498
pharmgkb	rs74315498
gwascentral	rs74315498
openSNP	rs74315498
23andMe	rs74315498
SNPshot	rs74315498
SNPdbe	rs74315498
MSV3d	rs74315498
GWAS Ctlg	rs74315498

Max Magnitude

0

OMIM	607379
Desc
Variant	0010
Related	also

ClinVar
Risk	rs74315498(T;T)
Alt	rs74315498(T;T)
Reference	Rs74315498(C;C)
Significance	Untested
Disease	Neurofibromatosis
Variation	info
Gene	NF2
CLNDBN	Neurofibromatosis, type 2
Reversed	0
HGVS	NC_000022.10:g.30067899C>T
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000023610.1, SCV000023610.1,