rs587776677

Orientation

plus

Stabilized

plus

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

Make rs587776677(-;-)

Make rs587776677(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

23825380

Gene

SMARCB1

is a	snp
is	mentioned by
dbSNP	rs587776677
dbSNP (classic)	rs587776677
ClinGen	rs587776677
ebi	rs587776677
HLI	rs587776677
Exac	rs587776677
Gnomad	rs587776677
Varsome	rs587776677
LitVar	rs587776677
Map	rs587776677
PheGenI	rs587776677
Biobank	rs587776677
1000 genomes	rs587776677
hgdp	rs587776677
ensembl	rs587776677
geneview	rs587776677
scholar	rs587776677
google	rs587776677
pharmgkb	rs587776677
gwascentral	rs587776677
openSNP	rs587776677
23andMe	rs587776677
SNPshot	rs587776677
SNPdbe	rs587776677
MSV3d	rs587776677
GWAS Ctlg	rs587776677

Max Magnitude

0

ClinVar
Risk	rs587776677(-;-)
Alt	rs587776677(-;-)
Reference	Rs587776677(A;A)
Significance	Pathogenic
Disease	Malignant rhabdoid tumor
Variation	info
Gene	SMARCB1
CLNDBN	Malignant rhabdoid tumor, somatic
Reversed	0
HGVS	NC_000022.10:g.24167567delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008486.4,