rs796053352

Orientation

plus

Stabilized

plus

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

Make rs796053352(A;G)

Make rs796053352(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

127658429

Gene

STXBP1

is a	snp
is	mentioned by
dbSNP	rs796053352
dbSNP (classic)	rs796053352
ClinGen	rs796053352
ebi	rs796053352
HLI	rs796053352
Exac	rs796053352
Gnomad	rs796053352
Varsome	rs796053352
LitVar	rs796053352
Map	rs796053352
PheGenI	rs796053352
Biobank	rs796053352
1000 genomes	rs796053352
hgdp	rs796053352
ensembl	rs796053352
geneview	rs796053352
scholar	rs796053352
google	rs796053352
pharmgkb	rs796053352
gwascentral	rs796053352
openSNP	rs796053352
23andMe	rs796053352
SNPshot	rs796053352
SNPdbe	rs796053352
MSV3d	rs796053352
GWAS Ctlg	rs796053352

Max Magnitude

0

ClinVar
Risk	rs796053352(G;G)
Alt	rs796053352(G;G)
Reference	Rs796053352(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	STXBP1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.130420708A>G
CLNSRC
CLNACC	RCV000189596.1,