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rs796052908

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs796052908(-;-)
Make rs796052908(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89327329
GeneMIR6766, POLG
is asnp
is mentioned by
dbSNPrs796052908
dbSNP (old)rs796052908
ClinGenrs796052908
ebirs796052908
HLIrs796052908
Exacrs796052908
Varsomers796052908
Maprs796052908
PheGenIrs796052908
Biobankrs796052908
1000 genomesrs796052908
hgdprs796052908
ensemblrs796052908
gopubmedrs796052908
geneviewrs796052908
scholarrs796052908
googlers796052908
pharmgkbrs796052908
gwascentralrs796052908
openSNPrs796052908
23andMers796052908
23andMe allrs796052908
SNP Nexus

SNPshotrs796052908
SNPdbers796052908
MSV3drs796052908
GWAS Ctlgrs796052908
Max Magnitude0
ClinVar
Risk rs796052908(-;-)
Alt rs796052908(-;-)
Reference Rs796052908(CT;CT)
Significance Pathogenic
Disease not provided Generalized epilepsy Global developmental delay Obesity
Variation info
Gene MIR6766 POLG
CLNDBN not provided Generalized epilepsy Global developmental delay Obesity
Reversed 1
HGVS NC_000015.9:g.89870560_89870561delAG
CLNSRC
CLNACC RCV000188674.2, RCV000449589.1,