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rs796052728

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052728(C;T)
Make rs796052728(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position88823746
GeneMEF2C
is asnp
is mentioned by
dbSNPrs796052728
ebirs796052728
HLIrs796052728
Exacrs796052728
Varsomers796052728
Maprs796052728
PheGenIrs796052728
hapmaprs796052728
1000 genomesrs796052728
hgdprs796052728
ensemblrs796052728
gopubmedrs796052728
geneviewrs796052728
scholarrs796052728
googlers796052728
pharmgkbrs796052728
gwascentralrs796052728
openSNPrs796052728
23andMers796052728
23andMe allrs796052728
SNP Nexus

SNPshotrs796052728
SNPdbers796052728
MSV3drs796052728
GWAS Ctlgrs796052728
Max Magnitude0
ClinVar
Risk rs796052728(T;T)
Alt rs796052728(T;T)
Reference rs796052728(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEF2C
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.88119563G>A
CLNSRC
CLNACC RCV000188145.2,