rs777826971

Orientation

plus

Stabilized

plus

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

Make rs777826971(G;T)

Make rs777826971(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

88729322

Gene

MEF2C

is a	snp
is	mentioned by
dbSNP	rs777826971
dbSNP (classic)	rs777826971
ClinGen	rs777826971
ebi	rs777826971
HLI	rs777826971
Exac	rs777826971
Gnomad	rs777826971
Varsome	rs777826971
LitVar	rs777826971
Map	rs777826971
PheGenI	rs777826971
Biobank	rs777826971
1000 genomes	rs777826971
hgdp	rs777826971
ensembl	rs777826971
geneview	rs777826971
scholar	rs777826971
google	rs777826971
pharmgkb	rs777826971
gwascentral	rs777826971
openSNP	rs777826971
23andMe	rs777826971
SNPshot	rs777826971
SNPdbe	rs777826971
MSV3d	rs777826971
GWAS Ctlg	rs777826971

Max Magnitude

0

ClinVar
Risk	rs777826971(A;A) rs777826971(T;T)
Alt	rs777826971(A;A) rs777826971(T;T)
Reference	Rs777826971(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MEF2C
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.88025139G>T
CLNSRC
CLNACC	RCV000481686.1,