rs786205649

Orientation

plus

Stabilized

plus

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

Make rs786205649(-;-)

Make rs786205649(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

33435176

Gene

SYNGAP1

is a	snp
is	mentioned by
dbSNP	rs786205649
dbSNP (classic)	rs786205649
ClinGen	rs786205649
ebi	rs786205649
HLI	rs786205649
Exac	rs786205649
Gnomad	rs786205649
Varsome	rs786205649
LitVar	rs786205649
Map	rs786205649
PheGenI	rs786205649
Biobank	rs786205649
1000 genomes	rs786205649
hgdp	rs786205649
ensembl	rs786205649
geneview	rs786205649
scholar	rs786205649
google	rs786205649
pharmgkb	rs786205649
gwascentral	rs786205649
openSNP	rs786205649
23andMe	rs786205649
SNPshot	rs786205649
SNPdbe	rs786205649
MSV3d	rs786205649
GWAS Ctlg	rs786205649

Max Magnitude

0

ClinVar
Risk	rs786205649(-;-)
Alt	rs786205649(-;-)
Reference	Rs786205649(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SYNGAP1
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.33402953delG
CLNSRC
CLNACC	RCV000171521.1,