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rs796052424

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052424(G;T)
Make rs796052424(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position145735333
GeneEPM2A, LOC100507557
is asnp
is mentioned by
dbSNPrs796052424
ebirs796052424
HLIrs796052424
Exacrs796052424
Varsomers796052424
Maprs796052424
PheGenIrs796052424
hapmaprs796052424
1000 genomesrs796052424
hgdprs796052424
ensemblrs796052424
gopubmedrs796052424
geneviewrs796052424
scholarrs796052424
googlers796052424
pharmgkbrs796052424
gwascentralrs796052424
openSNPrs796052424
23andMers796052424
23andMe allrs796052424
SNP Nexus

SNPshotrs796052424
SNPdbers796052424
MSV3drs796052424
GWAS Ctlgrs796052424
Max Magnitude0
ClinVar
Risk rs796052424(T;T)
Alt rs796052424(T;T)
Reference rs796052424(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene EPM2A LOC100507557
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.146056469C>A
CLNSRC
CLNACC RCV000187391.2,