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rs796052427

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052427(A;T)
Make rs796052427(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position145627534
GeneEPM2A
is asnp
is mentioned by
dbSNPrs796052427
ebirs796052427
HLIrs796052427
Exacrs796052427
Varsomers796052427
Maprs796052427
PheGenIrs796052427
hapmaprs796052427
1000 genomesrs796052427
hgdprs796052427
ensemblrs796052427
gopubmedrs796052427
geneviewrs796052427
scholarrs796052427
googlers796052427
pharmgkbrs796052427
gwascentralrs796052427
openSNPrs796052427
23andMers796052427
23andMe allrs796052427
SNP Nexus

SNPshotrs796052427
SNPdbers796052427
MSV3drs796052427
GWAS Ctlgrs796052427
Max Magnitude0
ClinVar
Risk rs796052427(T;T)
Alt rs796052427(T;T)
Reference rs796052427(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene EPM2A
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.145948670T>A
CLNSRC
CLNACC RCV000187395.1,