rs796052733

Orientation

minus

Stabilized

minus

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

Make rs796052733(C;T)

Make rs796052733(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

88731773

Gene

MEF2C

is a	snp
is	mentioned by
dbSNP	rs796052733
dbSNP (classic)	rs796052733
ClinGen	rs796052733
ebi	rs796052733
HLI	rs796052733
Exac	rs796052733
Gnomad	rs796052733
Varsome	rs796052733
LitVar	rs796052733
Map	rs796052733
PheGenI	rs796052733
Biobank	rs796052733
1000 genomes	rs796052733
hgdp	rs796052733
ensembl	rs796052733
geneview	rs796052733
scholar	rs796052733
google	rs796052733
pharmgkb	rs796052733
gwascentral	rs796052733
openSNP	rs796052733
23andMe	rs796052733
SNPshot	rs796052733
SNPdbe	rs796052733
MSV3d	rs796052733
GWAS Ctlg	rs796052733

Max Magnitude

0

ClinVar
Risk	rs796052733(T;T)
Alt	rs796052733(T;T)
Reference	Rs796052733(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MEF2C
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.88027590G>A
CLNSRC
CLNACC	RCV000188150.1,