rs886039520

Orientation

plus

Stabilized

plus

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

Make rs886039520(C;T)

Make rs886039520(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

22

Position

23833681

Gene

SMARCB1

is a	snp
is	mentioned by
dbSNP	rs886039520
dbSNP (classic)	rs886039520
ClinGen	rs886039520
ebi	rs886039520
HLI	rs886039520
Exac	rs886039520
Gnomad	rs886039520
Varsome	rs886039520
LitVar	rs886039520
Map	rs886039520
PheGenI	rs886039520
Biobank	rs886039520
1000 genomes	rs886039520
hgdp	rs886039520
ensembl	rs886039520
geneview	rs886039520
scholar	rs886039520
google	rs886039520
pharmgkb	rs886039520
gwascentral	rs886039520
openSNP	rs886039520
23andMe	rs886039520
SNPshot	rs886039520
SNPdbe	rs886039520
MSV3d	rs886039520
GWAS Ctlg	rs886039520

Max Magnitude

0

ClinVar
Risk	rs886039520(T;T)
Alt	rs886039520(T;T)
Reference	Rs886039520(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SMARCB1
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.24175868C>T
CLNSRC
CLNACC	RCV000255465.1,