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rs796052906

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052906(C;G)
Make rs796052906(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89325456
GenePOLG
is asnp
is mentioned by
dbSNPrs796052906
ebirs796052906
HLIrs796052906
Exacrs796052906
Varsomers796052906
Maprs796052906
PheGenIrs796052906
hapmaprs796052906
1000 genomesrs796052906
hgdprs796052906
ensemblrs796052906
gopubmedrs796052906
geneviewrs796052906
scholarrs796052906
googlers796052906
pharmgkbrs796052906
gwascentralrs796052906
openSNPrs796052906
23andMers796052906
23andMe allrs796052906
SNP Nexus

SNPshotrs796052906
SNPdbers796052906
MSV3drs796052906
GWAS Ctlgrs796052906
Max Magnitude0
ClinVar
Risk rs796052906(G;G)
Alt rs796052906(G;G)
Reference rs796052906(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89868687G>C
CLNSRC
CLNACC RCV000188671.1,