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rs796052733

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052733(C;T)
Make rs796052733(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position88731773
GeneMEF2C
is asnp
is mentioned by
dbSNPrs796052733
ebirs796052733
HLIrs796052733
Exacrs796052733
Varsomers796052733
Maprs796052733
PheGenIrs796052733
hapmaprs796052733
1000 genomesrs796052733
hgdprs796052733
ensemblrs796052733
gopubmedrs796052733
geneviewrs796052733
scholarrs796052733
googlers796052733
pharmgkbrs796052733
gwascentralrs796052733
openSNPrs796052733
23andMers796052733
23andMe allrs796052733
SNP Nexus

SNPshotrs796052733
SNPdbers796052733
MSV3drs796052733
GWAS Ctlgrs796052733
Max Magnitude0
ClinVar
Risk rs796052733(T;T)
Alt rs796052733(T;T)
Reference rs796052733(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEF2C
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.88027590G>A
CLNSRC
CLNACC RCV000188150.1,