rs779769475

Orientation

plus

Stabilized

plus

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

Make rs779769475(G;T)

Make rs779769475(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

23791820

Gene

SMARCB1

is a	snp
is	mentioned by
dbSNP	rs779769475
dbSNP (classic)	rs779769475
ClinGen	rs779769475
ebi	rs779769475
HLI	rs779769475
Exac	rs779769475
Gnomad	rs779769475
Varsome	rs779769475
LitVar	rs779769475
Map	rs779769475
PheGenI	rs779769475
Biobank	rs779769475
1000 genomes	rs779769475
hgdp	rs779769475
ensembl	rs779769475
geneview	rs779769475
scholar	rs779769475
google	rs779769475
pharmgkb	rs779769475
gwascentral	rs779769475
openSNP	rs779769475
23andMe	rs779769475
SNPshot	rs779769475
SNPdbe	rs779769475
MSV3d	rs779769475
GWAS Ctlg	rs779769475

Max Magnitude

0

ClinVar
Risk	rs779769475(A;A) rs779769475(T;T)
Alt	rs779769475(A;A) rs779769475(T;T)
Reference	Rs779769475(G;G)
Significance	Pathogenic
Disease	Rhabdoid tumor predisposition syndrome 1 Schwannomatosis not provided
Variation	info
Gene	SMARCB1
CLNDBN	Rhabdoid tumor predisposition syndrome 1 Schwannomatosis not provided
Reversed	0
HGVS	NC_000022.10:g.24134007G>T
CLNSRC
CLNACC	RCV000458462.1, RCV000490024.1,