rs796052728

Orientation

minus

Stabilized

minus

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

Make rs796052728(C;T)

Make rs796052728(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

88823746

Gene

MEF2C

is a	snp
is	mentioned by
dbSNP	rs796052728
dbSNP (classic)	rs796052728
ClinGen	rs796052728
ebi	rs796052728
HLI	rs796052728
Exac	rs796052728
Gnomad	rs796052728
Varsome	rs796052728
LitVar	rs796052728
Map	rs796052728
PheGenI	rs796052728
Biobank	rs796052728
1000 genomes	rs796052728
hgdp	rs796052728
ensembl	rs796052728
geneview	rs796052728
scholar	rs796052728
google	rs796052728
pharmgkb	rs796052728
gwascentral	rs796052728
openSNP	rs796052728
23andMe	rs796052728
SNPshot	rs796052728
SNPdbe	rs796052728
MSV3d	rs796052728
GWAS Ctlg	rs796052728

Max Magnitude

0

ClinVar
Risk	rs796052728(T;T)
Alt	rs796052728(T;T)
Reference	Rs796052728(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MEF2C
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.88119563G>A
CLNSRC
CLNACC	RCV000188145.3,