Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052735

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052735(C;C)
Make rs796052735(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position88823786
GeneMEF2C
is asnp
is mentioned by
dbSNPrs796052735
ebirs796052735
HLIrs796052735
Exacrs796052735
Varsomers796052735
Maprs796052735
PheGenIrs796052735
hapmaprs796052735
1000 genomesrs796052735
hgdprs796052735
ensemblrs796052735
gopubmedrs796052735
geneviewrs796052735
scholarrs796052735
googlers796052735
pharmgkbrs796052735
gwascentralrs796052735
openSNPrs796052735
23andMers796052735
23andMe allrs796052735
SNP Nexus

SNPshotrs796052735
SNPdbers796052735
MSV3drs796052735
GWAS Ctlgrs796052735
Max Magnitude0
ClinVar
Risk rs796052735(C;C)
Alt rs796052735(C;C)
Reference rs796052735(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEF2C
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.88119603C>G
CLNSRC
CLNACC RCV000188153.1,