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rs796052725

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052725(C;T)
Make rs796052725(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position88751923
GeneMEF2C
is asnp
is mentioned by
dbSNPrs796052725
ebirs796052725
HLIrs796052725
Exacrs796052725
Varsomers796052725
Maprs796052725
PheGenIrs796052725
hapmaprs796052725
1000 genomesrs796052725
hgdprs796052725
ensemblrs796052725
gopubmedrs796052725
geneviewrs796052725
scholarrs796052725
googlers796052725
pharmgkbrs796052725
gwascentralrs796052725
openSNPrs796052725
23andMers796052725
23andMe allrs796052725
SNP Nexus

SNPshotrs796052725
SNPdbers796052725
MSV3drs796052725
GWAS Ctlgrs796052725
Max Magnitude0
ClinVar
Risk rs796052725(T;T)
Alt rs796052725(T;T)
Reference rs796052725(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEF2C
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.88047740G>A
CLNSRC
CLNACC RCV000188141.2,