rs267607072

Orientation

plus

Stabilized

plus

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

Make rs267607072(A;T)

Make rs267607072(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

23787261

Gene

SMARCB1

is a	snp
is	mentioned by
dbSNP	rs267607072
dbSNP (classic)	rs267607072
ClinGen	rs267607072
ebi	rs267607072
HLI	rs267607072
Exac	rs267607072
Gnomad	rs267607072
Varsome	rs267607072
LitVar	rs267607072
Map	rs267607072
PheGenI	rs267607072
Biobank	rs267607072
1000 genomes	rs267607072
hgdp	rs267607072
ensembl	rs267607072
geneview	rs267607072
scholar	rs267607072
google	rs267607072
pharmgkb	rs267607072
gwascentral	rs267607072
openSNP	rs267607072
23andMe	rs267607072
SNPshot	rs267607072
SNPdbe	rs267607072
MSV3d	rs267607072
GWAS Ctlg	rs267607072

Max Magnitude

0

ClinVar
Risk	rs267607072(T;T)
Alt	rs267607072(T;T)
Reference	Rs267607072(A;A)
Significance	Pathogenic
Disease	Schwannomatosis 1
Variation	info
Gene	SMARCB1
CLNDBN	Schwannomatosis 1
Reversed	0
HGVS	NC_000022.10:g.24129448A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008496.5,