rs1085307871

Orientation

plus

Stabilized

plus

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

Make rs1085307871(T;T)

Chromosome

6

Position

33432769

Gene

SYNGAP1

is a	snp
is	mentioned by
dbSNP	rs1085307871
dbSNP (classic)	rs1085307871
ClinGen	rs1085307871
ebi	rs1085307871
HLI	rs1085307871
Exac	rs1085307871
Gnomad	rs1085307871
Varsome	rs1085307871
LitVar	rs1085307871
Map	rs1085307871
PheGenI	rs1085307871
Biobank	rs1085307871
1000 genomes	rs1085307871
hgdp	rs1085307871
ensembl	rs1085307871
geneview	rs1085307871
scholar	rs1085307871
google	rs1085307871
pharmgkb	rs1085307871
gwascentral	rs1085307871
openSNP	rs1085307871
23andMe	rs1085307871
SNPshot	rs1085307871
SNPdbe	rs1085307871
MSV3d	rs1085307871
GWAS Ctlg	rs1085307871

Max Magnitude

8.8

ClinVar
Risk	rs1085307871(T;T)
Alt	rs1085307871(T;T)
Reference	Rs1085307871(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SYNGAP1
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.33400546C>T
CLNSRC
CLNACC	RCV000489135.1,