rs587780474

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;G)	8.8	Mental retardation, type 5; SYNGAP1-related
(G;G)	0	common in clinvar

Make rs587780474(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

33443154

Gene

SYNGAP1

is a	snp
is	mentioned by
dbSNP	rs587780474
dbSNP (classic)	rs587780474
ClinGen	rs587780474
ebi	rs587780474
HLI	rs587780474
Exac	rs587780474
Gnomad	rs587780474
Varsome	rs587780474
LitVar	rs587780474
Map	rs587780474
PheGenI	rs587780474
Biobank	rs587780474
1000 genomes	rs587780474
hgdp	rs587780474
ensembl	rs587780474
geneview	rs587780474
scholar	rs587780474
google	rs587780474
pharmgkb	rs587780474
gwascentral	rs587780474
openSNP	rs587780474
23andMe	rs587780474
SNPshot	rs587780474
SNPdbe	rs587780474
MSV3d	rs587780474
GWAS Ctlg	rs587780474

Max Magnitude

8.8

ClinVar
Risk	rs587780474(-;-)
Alt	rs587780474(-;-)
Reference	Rs587780474(G;G)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	SYNGAP1
CLNDBN	Mental retardation, autosomal dominant 5
Reversed	0
HGVS	NC_000006.11:g.33410931delG
CLNSRC
CLNACC	RCV000118568.1,