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rs375935084

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs375935084(A;A)
Make rs375935084(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89321217
GenePOLG
is asnp
is mentioned by
dbSNPrs375935084
ebirs375935084
HLIrs375935084
Exacrs375935084
Varsomers375935084
Maprs375935084
PheGenIrs375935084
hapmaprs375935084
1000 genomesrs375935084
hgdprs375935084
ensemblrs375935084
gopubmedrs375935084
geneviewrs375935084
scholarrs375935084
googlers375935084
pharmgkbrs375935084
gwascentralrs375935084
openSNPrs375935084
23andMers375935084
23andMe allrs375935084
SNP Nexus

SNPshotrs375935084
SNPdbers375935084
MSV3drs375935084
GWAS Ctlgrs375935084
Max Magnitude0
ClinVar
Risk rs375935084(A;A)
Alt rs375935084(A;A)
Reference rs375935084(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89864448G>A
CLNSRC
CLNACC RCV000188677.1,