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rs796052428

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052428(C;T)
Make rs796052428(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position145627510
GeneEPM2A
is asnp
is mentioned by
dbSNPrs796052428
dbSNP (old)rs796052428
ClinGenrs796052428
ebirs796052428
HLIrs796052428
Exacrs796052428
Gnomadrs796052428
Varsomers796052428
Maprs796052428
PheGenIrs796052428
Biobankrs796052428
1000 genomesrs796052428
hgdprs796052428
ensemblrs796052428
gopubmedrs796052428
geneviewrs796052428
scholarrs796052428
googlers796052428
pharmgkbrs796052428
gwascentralrs796052428
openSNPrs796052428
23andMers796052428
23andMe allrs796052428
SNP Nexus

SNPshotrs796052428
SNPdbers796052428
MSV3drs796052428
GWAS Ctlgrs796052428
Max Magnitude0
ClinVar
Risk rs796052428(T;T)
Alt rs796052428(T;T)
Reference Rs796052428(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EPM2A
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.145948646G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000187397.1,