Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052887

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052887(A;A)
Make rs796052887(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89322748
GenePOLG
is asnp
is mentioned by
dbSNPrs796052887
ebirs796052887
HLIrs796052887
Exacrs796052887
Varsomers796052887
Maprs796052887
PheGenIrs796052887
hapmaprs796052887
1000 genomesrs796052887
hgdprs796052887
ensemblrs796052887
gopubmedrs796052887
geneviewrs796052887
scholarrs796052887
googlers796052887
pharmgkbrs796052887
gwascentralrs796052887
openSNPrs796052887
23andMers796052887
23andMe allrs796052887
SNP Nexus

SNPshotrs796052887
SNPdbers796052887
MSV3drs796052887
GWAS Ctlgrs796052887
Max Magnitude0
ClinVar
Risk rs796052887(A;A)
Alt rs796052887(A;A)
Reference rs796052887(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89865979C>T
CLNSRC
CLNACC RCV000188575.2,