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rs181860632

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs181860632(A;A)
Make rs181860632(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89319065
GenePOLG
is asnp
is mentioned by
dbSNPrs181860632
ebirs181860632
HLIrs181860632
Exacrs181860632
Varsomers181860632
Maprs181860632
PheGenIrs181860632
hapmaprs181860632
1000 genomesrs181860632
hgdprs181860632
ensemblrs181860632
gopubmedrs181860632
geneviewrs181860632
scholarrs181860632
googlers181860632
pharmgkbrs181860632
gwascentralrs181860632
openSNPrs181860632
23andMers181860632
23andMe allrs181860632
SNP Nexus

SNPshotrs181860632
SNPdbers181860632
MSV3drs181860632
GWAS Ctlgrs181860632
Max Magnitude0
ClinVar
Risk rs181860632(A;A)
Alt rs181860632(A;A)
Reference rs181860632(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89862296G>A
CLNSRC
CLNACC RCV000188603.1,