rs796052735

Orientation

minus

Stabilized

minus

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

Make rs796052735(C;C)

Make rs796052735(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

88823786

Gene

MEF2C

is a	snp
is	mentioned by
dbSNP	rs796052735
dbSNP (classic)	rs796052735
ClinGen	rs796052735
ebi	rs796052735
HLI	rs796052735
Exac	rs796052735
Gnomad	rs796052735
Varsome	rs796052735
LitVar	rs796052735
Map	rs796052735
PheGenI	rs796052735
Biobank	rs796052735
1000 genomes	rs796052735
hgdp	rs796052735
ensembl	rs796052735
geneview	rs796052735
scholar	rs796052735
google	rs796052735
pharmgkb	rs796052735
gwascentral	rs796052735
openSNP	rs796052735
23andMe	rs796052735
SNPshot	rs796052735
SNPdbe	rs796052735
MSV3d	rs796052735
GWAS Ctlg	rs796052735

Max Magnitude

0

ClinVar
Risk	rs796052735(C;C)
Alt	rs796052735(C;C)
Reference	Rs796052735(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MEF2C
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.88119603C>G
CLNSRC
CLNACC	RCV000188153.1,