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rs139717885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139717885(A;A)
Make rs139717885(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position89325610
GenePOLG
is asnp
is mentioned by
dbSNPrs139717885
dbSNP (old)rs139717885
ClinGenrs139717885
ebirs139717885
HLIrs139717885
Exacrs139717885
Gnomadrs139717885
Varsomers139717885
Maprs139717885
PheGenIrs139717885
Biobankrs139717885
1000 genomesrs139717885
hgdprs139717885
ensemblrs139717885
gopubmedrs139717885
geneviewrs139717885
scholarrs139717885
googlers139717885
pharmgkbrs139717885
gwascentralrs139717885
openSNPrs139717885
23andMers139717885
23andMe allrs139717885
SNPshotrs139717885
SNPdbers139717885
MSV3drs139717885
GWAS Ctlgrs139717885
Max Magnitude0
ClinVar
Risk rs139717885(A;A)
Alt rs139717885(A;A)
Reference Rs139717885(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89868841G>A
CLNSRC
CLNACC RCV000438492.1,