rs387906811

Orientation

plus

Stabilized

plus

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

Make rs387906811(C;T)

Make rs387906811(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

23791805

Gene

SMARCB1

is a	snp
is	mentioned by
dbSNP	rs387906811
dbSNP (classic)	rs387906811
ClinGen	rs387906811
ebi	rs387906811
HLI	rs387906811
Exac	rs387906811
Gnomad	rs387906811
Varsome	rs387906811
LitVar	rs387906811
Map	rs387906811
PheGenI	rs387906811
Biobank	rs387906811
1000 genomes	rs387906811
hgdp	rs387906811
ensembl	rs387906811
geneview	rs387906811
scholar	rs387906811
google	rs387906811
pharmgkb	rs387906811
gwascentral	rs387906811
openSNP	rs387906811
23andMe	rs387906811
SNPshot	rs387906811
SNPdbe	rs387906811
MSV3d	rs387906811
GWAS Ctlg	rs387906811

Max Magnitude

0

ClinVar
Risk	rs387906811(T;T)
Alt	rs387906811(T;T)
Reference	Rs387906811(C;C)
Significance	Pathogenic
Disease	Schwannomatosis 1
Variation	info
Gene	SMARCB1
CLNDBN	Schwannomatosis 1
Reversed	0
HGVS	NC_000022.10:g.24133992C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023122.6,