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rs796052434

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052434(A;A)
Make rs796052434(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position145735411
GeneEPM2A, LOC100507557
is asnp
is mentioned by
dbSNPrs796052434
ebirs796052434
HLIrs796052434
Exacrs796052434
Varsomers796052434
Maprs796052434
PheGenIrs796052434
hapmaprs796052434
1000 genomesrs796052434
hgdprs796052434
ensemblrs796052434
gopubmedrs796052434
geneviewrs796052434
scholarrs796052434
googlers796052434
pharmgkbrs796052434
gwascentralrs796052434
openSNPrs796052434
23andMers796052434
23andMe allrs796052434
SNP Nexus

SNPshotrs796052434
SNPdbers796052434
MSV3drs796052434
GWAS Ctlgrs796052434
Max Magnitude0
ClinVar
Risk rs796052434(A;A)
Alt rs796052434(A;A)
Reference rs796052434(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EPM2A LOC100507557
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.146056547C>T
CLNSRC
CLNACC RCV000187405.1,