rs796052724

Orientation

minus

Stabilized

minus

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

Make rs796052724(A;A)

Make rs796052724(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

88804598

Gene

MEF2C

is a	snp
is	mentioned by
dbSNP	rs796052724
dbSNP (classic)	rs796052724
ClinGen	rs796052724
ebi	rs796052724
HLI	rs796052724
Exac	rs796052724
Gnomad	rs796052724
Varsome	rs796052724
LitVar	rs796052724
Map	rs796052724
PheGenI	rs796052724
Biobank	rs796052724
1000 genomes	rs796052724
hgdp	rs796052724
ensembl	rs796052724
geneview	rs796052724
scholar	rs796052724
google	rs796052724
pharmgkb	rs796052724
gwascentral	rs796052724
openSNP	rs796052724
23andMe	rs796052724
SNPshot	rs796052724
SNPdbe	rs796052724
MSV3d	rs796052724
GWAS Ctlg	rs796052724

Max Magnitude

0

ClinVar
Risk	rs796052724(A;A)
Alt	rs796052724(A;A)
Reference	Rs796052724(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MEF2C
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.88100415C>T
CLNSRC
CLNACC	RCV000188140.1,