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rs796052888

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052888(A;A)
Make rs796052888(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89321776
GenePOLG
is asnp
is mentioned by
dbSNPrs796052888
ebirs796052888
HLIrs796052888
Exacrs796052888
Varsomers796052888
Maprs796052888
PheGenIrs796052888
hapmaprs796052888
1000 genomesrs796052888
hgdprs796052888
ensemblrs796052888
gopubmedrs796052888
geneviewrs796052888
scholarrs796052888
googlers796052888
pharmgkbrs796052888
gwascentralrs796052888
openSNPrs796052888
23andMers796052888
23andMe allrs796052888
SNP Nexus

SNPshotrs796052888
SNPdbers796052888
MSV3drs796052888
GWAS Ctlgrs796052888
Max Magnitude0
ClinVar
Risk rs796052888(A;A)
Alt rs796052888(A;A)
Reference rs796052888(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89865007C>T
CLNSRC
CLNACC RCV000188583.1,