rs752059006

Orientation

plus

Stabilized

plus

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

Make rs752059006(C;C)

Make rs752059006(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

23353788

Gene

SACS

is a	snp
is	mentioned by
dbSNP	rs752059006
dbSNP (classic)	rs752059006
ClinGen	rs752059006
ebi	rs752059006
HLI	rs752059006
Exac	rs752059006
Gnomad	rs752059006
Varsome	rs752059006
LitVar	rs752059006
Map	rs752059006
PheGenI	rs752059006
Biobank	rs752059006
1000 genomes	rs752059006
hgdp	rs752059006
ensembl	rs752059006
geneview	rs752059006
scholar	rs752059006
google	rs752059006
pharmgkb	rs752059006
gwascentral	rs752059006
openSNP	rs752059006
23andMe	rs752059006
SNPshot	rs752059006
SNPdbe	rs752059006
MSV3d	rs752059006
GWAS Ctlg	rs752059006

Max Magnitude

0

ClinVar
Risk	rs752059006(A;A) rs752059006(C;C)
Alt	rs752059006(A;A) rs752059006(C;C)
Reference	Rs752059006(G;G)
Significance	Pathogenic
Disease	not provided Abnormality of brain morphology
Variation	info
Gene	SACS
CLNDBN	not provided Abnormality of brain morphology
Reversed	0
HGVS	NC_000013.10:g.23927927G>A
CLNSRC
CLNACC	RCV000393719.1, RCV000454220.1,