rs797045989

Orientation

plus

Stabilized

plus

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

Make rs797045989(A;G)

Make rs797045989(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

23833672

Gene

SMARCB1

is a	snp
is	mentioned by
dbSNP	rs797045989
dbSNP (classic)	rs797045989
ClinGen	rs797045989
ebi	rs797045989
HLI	rs797045989
Exac	rs797045989
Gnomad	rs797045989
Varsome	rs797045989
LitVar	rs797045989
Map	rs797045989
PheGenI	rs797045989
Biobank	rs797045989
1000 genomes	rs797045989
hgdp	rs797045989
ensembl	rs797045989
geneview	rs797045989
scholar	rs797045989
google	rs797045989
pharmgkb	rs797045989
gwascentral	rs797045989
openSNP	rs797045989
23andMe	rs797045989
SNPshot	rs797045989
SNPdbe	rs797045989
MSV3d	rs797045989
GWAS Ctlg	rs797045989

Max Magnitude

0

ClinVar
Risk	rs797045989(G;G)
Alt	rs797045989(G;G)
Reference	Rs797045989(A;A)
Significance	Probable-Pathogenic
Disease	Mental retardation
Variation	info
Gene	SMARCB1
CLNDBN	Mental retardation, autosomal dominant 15
Reversed	0
HGVS	NC_000022.10:g.24175859A>G
CLNSRC
CLNACC	RCV000194966.1,