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rs1064797310

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome5
Position88804597
GeneMEF2C
is asnp
is mentioned by
dbSNPrs1064797310
dbSNP (old)rs1064797310
ClinGenrs1064797310
ebirs1064797310
HLIrs1064797310
Exacrs1064797310
Gnomadrs1064797310
Varsomers1064797310
Maprs1064797310
PheGenIrs1064797310
Biobankrs1064797310
1000 genomesrs1064797310
hgdprs1064797310
ensemblrs1064797310
gopubmedrs1064797310
geneviewrs1064797310
scholarrs1064797310
googlers1064797310
pharmgkbrs1064797310
gwascentralrs1064797310
openSNPrs1064797310
23andMers1064797310
23andMe allrs1064797310
SNPshotrs1064797310
SNPdbers1064797310
MSV3drs1064797310
GWAS Ctlgrs1064797310
Max Magnitude0
ClinVar
Risk rs1064797310(T;T)
Alt rs1064797310(T;T)
Reference Rs1064797310(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEF2C
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.88100414C>A
CLNSRC
CLNACC RCV000487816.1,