rs796052725

Orientation

minus

Stabilized

minus

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

Make rs796052725(C;T)

Make rs796052725(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

88751923

Gene

MEF2C

is a	snp
is	mentioned by
dbSNP	rs796052725
dbSNP (classic)	rs796052725
ClinGen	rs796052725
ebi	rs796052725
HLI	rs796052725
Exac	rs796052725
Gnomad	rs796052725
Varsome	rs796052725
LitVar	rs796052725
Map	rs796052725
PheGenI	rs796052725
Biobank	rs796052725
1000 genomes	rs796052725
hgdp	rs796052725
ensembl	rs796052725
geneview	rs796052725
scholar	rs796052725
google	rs796052725
pharmgkb	rs796052725
gwascentral	rs796052725
openSNP	rs796052725
23andMe	rs796052725
SNPshot	rs796052725
SNPdbe	rs796052725
MSV3d	rs796052725
GWAS Ctlg	rs796052725

Max Magnitude

0

ClinVar
Risk	rs796052725(T;T)
Alt	rs796052725(T;T)
Reference	Rs796052725(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MEF2C
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.88047740G>A
CLNSRC
CLNACC	RCV000188141.2,