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rs796052724

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052724(A;A)
Make rs796052724(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position88804598
GeneMEF2C
is asnp
is mentioned by
dbSNPrs796052724
ebirs796052724
HLIrs796052724
Exacrs796052724
Varsomers796052724
Maprs796052724
PheGenIrs796052724
hapmaprs796052724
1000 genomesrs796052724
hgdprs796052724
ensemblrs796052724
gopubmedrs796052724
geneviewrs796052724
scholarrs796052724
googlers796052724
pharmgkbrs796052724
gwascentralrs796052724
openSNPrs796052724
23andMers796052724
23andMe allrs796052724
SNP Nexus

SNPshotrs796052724
SNPdbers796052724
MSV3drs796052724
GWAS Ctlgrs796052724
Max Magnitude0
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,