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rs752892262

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752892262(A;A)
Make rs752892262(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89333267
GeneLOC105370962, POLG
is asnp
is mentioned by
dbSNPrs752892262
ClinGenrs752892262
ebirs752892262
HLIrs752892262
Exacrs752892262
Varsomers752892262
Maprs752892262
PheGenIrs752892262
hapmaprs752892262
1000 genomesrs752892262
hgdprs752892262
ensemblrs752892262
gopubmedrs752892262
geneviewrs752892262
scholarrs752892262
googlers752892262
pharmgkbrs752892262
gwascentralrs752892262
openSNPrs752892262
23andMers752892262
23andMe allrs752892262
SNP Nexus

SNPshotrs752892262
SNPdbers752892262
MSV3drs752892262
GWAS Ctlgrs752892262
Max Magnitude0
ClinVar
Risk rs752892262(A;A)
Alt rs752892262(A;A)
Reference Rs752892262(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89876498G>A
CLNSRC
CLNACC RCV000188636.1,