rs1060501395

Orientation

minus

Stabilized

minus

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

Make rs1060501395(C;T)

Make rs1060501395(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

40636451

Gene

SMARCE1

is a	snp
is	mentioned by
dbSNP	rs1060501395
dbSNP (classic)	rs1060501395
ClinGen	rs1060501395
ebi	rs1060501395
HLI	rs1060501395
Exac	rs1060501395
Gnomad	rs1060501395
Varsome	rs1060501395
LitVar	rs1060501395
Map	rs1060501395
PheGenI	rs1060501395
Biobank	rs1060501395
1000 genomes	rs1060501395
hgdp	rs1060501395
ensembl	rs1060501395
geneview	rs1060501395
scholar	rs1060501395
google	rs1060501395
pharmgkb	rs1060501395
gwascentral	rs1060501395
openSNP	rs1060501395
23andMe	rs1060501395
SNPshot	rs1060501395
SNPdbe	rs1060501395
MSV3d	rs1060501395
GWAS Ctlg	rs1060501395

Max Magnitude

0

ClinVar
Risk	rs1060501395(T;T)
Alt	rs1060501395(T;T)
Reference	Rs1060501395(C;C)
Significance	Pathogenic
Disease	Meningioma
Variation	info
Gene	SMARCE1
CLNDBN	Meningioma, familial
Reversed	1
HGVS	NC_000017.10:g.38792703G>A
CLNSRC
CLNACC	RCV000466082.1,